• Skip to primary navigation
  • Skip to main content
  • +1-757-224-0177
  • Contact Us
  • MyFDA Login
  • COVID-19 PPE
  • English
    • Español
    • Italiano
    • Deutsch
    • Français
    • 中文
    • Portuguese
    • 日本語
Registrar

Registrar

Assistance with U.S. FDA Regulations

  • English
    • Español
    • Italiano
    • Deutsch
    • Français
    • 中文
    • Portuguese
    • 日本語
  • FDA Registration
  • Services
    • FDA Registration
    • Cosmetics FDA Registration
    • U.S. FDA Detention Assistance
    • Food Safety and FSMA
    • FDA Labeling
    • UDI and GUDID
    • Master Files
    • GACC Registration
    • Unique Facility Identifier (UFI)
    • U.S. FDA Export Certificate Requirements
    • TTB Registration
  • Products
    • FDA Compliance Monitor
      • Buyer Insights
      • Marketplace
      • Exporter Marketplace
    • Cosmetri
    • A la Calc
    • Online Training
  • Our Brands
    • Cosmetri
    • A la Calc
  • Industries
    • Food and Beverages
    • Dietary Supplements
    • Medical Devices
    • Drugs
    • Cosmetics
    • Other
  • Resources
    • Resources
    • Regulatory News
    • Events / Webinars
    • Partners
    • Free Tools
  • About Us
    • About
    • Contact Us
    • Careers

Are You Ready for an FDA Inspection?

Registrar Corp is offering Virtual Inspection Preparation Assistance during COVID-19.

Get Help Now

Magnifying Glass
Are You Prepared
For A U.S. FDA Inspection?

When you register with the U.S. Food and Drug Administration (FDA), you consent to an FDA inspection at any time. FDA may choose to conduct a routine inspection of a facility. In addition, FDA may also inspect any U.S. importer for Foreign Supplier Verification Program (FSVP) compliance of each food and beverage product from foreign suppliers.

Registrar Corp can dispatch a Food Safety Specialist to help your facility prepare for an FDA inspection.

Order a Mock FDA Food Facility Inspection
Order a Mock FSVP Inspection

What can you expect from an upcoming inspection?

FDA Food Facility Inspection

Assesses the following during a 2-5 day period:

  • FDA-registered food facilities must follow Current Good Manufacturing Practices (CGMPs) that address aspects such as:
    • Employee Hygiene and Training
    • Plant Construction and Design
    • Cleaning and Sanitation Procedures
    • Raw Materials & Ingredients
    • Manufacturing Operations
  • The Preventive Controls rules require facilities to implement Hazard Analysis and Risk-Based Preventive Controls (HARPC) plans, which include aspects such as:
    • An analysis of known and reasonably foreseeable food hazards
    • Preventive controls for identified hazards
    • Adequate monitoring procedures for preventive controls
    • Supply-Chain Program
    • Recall Plan

FSVP Inspection

FDA is authorized to collect FSVP records and other relevant information during an FSVP inspection. The information requested can be associated to the following, as applicable:

  • Eligibility for very small importers (i.e., financial records, calculations, etc.)
  • Determination that a food product is within the scope, under the regulatory oversight and in compliance with the food safety requirements of a country that has an agreement with FDA
  • Evaluation of the foreign supplier for approval (i.e., supplier performance and risk posed by the food)
  • Hazard Analysis of the food
  • Determination and conduct of verification activities
  • Supplier written assurances
  • Corrective actions taken when food safety issues were discovered, if applicable
  • Written procedures for conducting FSVP-related activities
  • FSVP supporting documents (e.g., product descriptions/specifications, labels, supplier's food safety plan, food safety records, testing and/or audit reports, etc.)
  • A Qualified Individual's merits
  • And more...

Registrar Corp Makes Compliance Easy

Registrar Corp can dispatch a Food Safety Specialist to help you prepare for an FDA inspection.

A Mock FDA Food Facility Inspection includes:

A complete review of your food safety documentation

A thorough assessment of your facility's compliance with regulatory requirements

Virtual or onsite expert assistance from a Food Safety Specialist

A Mock FSVP Inspection includes:

Review of all FSVP documentation

Assessment of documentation identification of incomplete, inaccurate or missing documents

Virtual expert assistance from Food Safety Specialist

1Company Information
2Payment Information
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • (11 Digit number given by FDA)
  • Amount Due

  • Amount Due
    Total
  • Bill to:

  • Price: $695.00
  • This field is hidden when viewing the form
  • (Valid until December 31,  )
  • (Valid until December 31,  )
  • (Valid until December 31,  )
  • (valid until )
    includes FDA Compliance and Shipment Monitoring
  • Based on your specified suppliers, Registrar Corp recommends a block of . This value can be changed below.

  • (valid until )
  • (valid until )
  • This field is hidden when viewing the form
  • Registrar Corp recommends having the following documents for this submission:

    For the product:

    • Product name, number and size of retail containers, batch and lot numbers, any product identification codes, IFN number (if previously notified to FDA)
    • Countries in which currently marketed and duration
    • Quantity intended to be introduced to US market (by weight).
    • “Use by” date if in current inventory. If not in current inventory, the date you plan to introduce it into U.S. commerce. Indicate if it will be a one-time shipment or multiple shipments.
    • Name and location of manufacturing facilities
    • Distribution plan down to retail level, if available
    • Full quantitative formulation, list of all ingredients, amount of each ingredient per absolute amount (such as mg/kg or g/L)
    • Copy of the product label
    • Description of the product packaging
    • Summary of finished product testing results for most recent batch/lot at each facility:
      • Level of each nutrient required by 21 CFR 107.100
      • Level of any other nutrient added by the manufacturer in units per 100 kcal
      • Explanation of any deviation for a specialized formula that may not meet all requirements but is appropriate for dietary management of a specific disease or disorder
    • For powdered formula, a summary of finished product testing results for the most recent batch/lot at each facility:
      • For Cronobacter : 30 samples, with each sample being 10 grams
      • For Salmonella : 60 samples, with each sample being 25 grams
      • Description of test method used and copy of the method (e.g., certificate of
        analysis with information listed in 21 CFR 117.165(b)(2) from a qualified laboratory)

    For each manufacturing facility:

    • Certification of established current GMP designed to prevent adulteration, including quality control procedures and in-process controls, and testing required under the cGMP
    • Schematic diagram (i.e. process flow diagram) with processing times and temperatures, written narrative that includes a summary of process flow, heating and processing conditions, and critical control points
    • FDA Food Facility Registration Number
    • If facility has not received an FDA inspection:
      • Date of last inspection by the relevant government authority, or
      • Third party audit conducted by a qualified auditor on behalf of the government authority
      • Summary of the findings, standards/regulations against which the inspection was conducted, and any actions taken by the manufacturer in response
  • $0.00
  • please wait
  • American Express
    Discover
    MasterCard
    Visa
    Supported Credit Cards: American Express, Discover, MasterCard, Visa
     
  • This field is hidden when viewing the form
    MM slash DD slash YYYY

Solutions

FDA Registration

FDA Compliance Monitor

FDA Labeling

View All

About

About Us

Resources

Free Tools

Fees

Contact Us

 

Reviews

Locations

Events

Associations

Careers

Phone: +1-757-224-0177

Fax: +1-757-224-0179

[email protected]

© 2025 Registrar Corp

144 Research Drive Hampton, Virginia 23666 USA
Terms of Use | Privacy Policy

  • English
    • Español
    • Italiano
    • Deutsch
    • Français
    • 中文
    • Portuguese
    • 日本語
    • Back
  • FDA Registration
  • Services
    • FDA Registration
    • Cosmetics FDA Registration
    • U.S. FDA Detention Assistance
    • Food Safety and FSMA
    • FDA Labeling
    • UDI and GUDID
    • Master Files
    • GACC Registration
    • Unique Facility Identifier (UFI)
    • U.S. FDA Export Certificate Requirements
    • TTB Registration
    • Back
  • Products
    • FDA Compliance Monitor
      • Buyer Insights
      • Marketplace
      • Exporter Marketplace
      • Back
    • Cosmetri
    • A la Calc
    • Online Training
    • Back
  • Our Brands
    • Cosmetri
    • A la Calc
    • Back
  • Industries
    • Food and Beverages
    • Dietary Supplements
    • Medical Devices
    • Drugs
    • Cosmetics
    • Other
    • Back
  • Resources
    • Resources
    • Regulatory News
    • Events / Webinars
    • Partners
    • Free Tools
    • Back
  • About Us
    • About
    • Contact Us
    • Careers
    • Back

FDA has cancelled thousands of registrations that were not properly renewed or did not include
an accurate Unique Facility Identifier (UFI). If you need immediate assistance, Registrar Corp can help.

Notice: Medical Device and Drug establishments that did not renew their FDA registrations in   must re-register.


Get Help Now

FDA-registered facilities must renew their registrations by December 31,  

Medical Device and Drug establishments must renew their registrations by December 31,  

Renew Now

Reminder

The U.S. Food and Drug Administration (FDA) requires that all registered food, medical device, and drug facilities renew their FDA registration between October 1 and December 31,

Renew Now

Notice

The U.S. FDA Registration Renewal period CLOSED on December 31,

If you did not renew by the deadline, you must re-register with FDA.

Re-register or verify that your registration was renewed for :

Re-Register
Verify

Limited Time Offer

Get 18 Months of Registration and U.S. Agent service for the price of 12 when you sign up today.

Get Started
Open Modal