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The Gerard Group FDA Inspection Record

FEI 3006687916 · Inspections, Form 483s, warning letters and import refusals

The Gerard Group is an FDA-inspected facility (FEI 3006687916) located in Courtland, VA, US. RegDataLab tracks 3 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Nov 6, 2023: No Action Indicated (NAI)
Inspections on record
3 (3 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Nov 6, 2023No Action Indicated (NAI)No citations listed
Sep 13, 2021No Action Indicated (NAI)No citations listed
Oct 21, 2009No Action Indicated (NAI)No citations listed

Facility details

Company
The Gerard Group
Location
Courtland, VA (US)
Source
inspections

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.