Ethypharm FDA Inspection Record

FEI 3004715600 · Inspections, Form 483s, warning letters and import refusals

Ethypharm is an FDA-registered facility (FEI 3004715600) located in Le Grand Quevilly, FR. Registered operations: ANALYSIS; MANUFACTURE. RegDataLab tracks 5 FDA inspections at this facility.

Reviewing Ethypharm as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Ethypharm yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

What FDA found at this site

Latest inspection
Oct 7, 2022: Voluntary Action Indicated (VAI)
Inspections on record
5 (4 VAI, 1 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
Oct 7, 2022Voluntary Action Indicated (VAI)No citations listed
Nov 5, 2020Voluntary Action Indicated (VAI)No citations listed
Dec 5, 2014No Action Indicated (NAI)No citations listed
Oct 19, 2012Voluntary Action Indicated (VAI)Lack of written stability program (21 CFR 211.166(a))
Feb 19, 2009Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Ethypharm
Location
Le Grand Quevilly (FR)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; MANUFACTURE
Source
decrs

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