Ethypharm FDA Inspection Record

FEI 3002807933 ยท Inspections, Form 483s, warning letters and import refusals

Ethypharm is an FDA-registered facility (FEI 3002807933) located in Centre Val de Loire 28170, FR. Registered operations: ANALYSIS; MANUFACTURE. RegDataLab tracks 6 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Nov 16, 2023: Voluntary Action Indicated (VAI)
Inspections on record
6 (5 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
Import refusals
1

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 16, 2023Voluntary Action Indicated (VAI)No citations listed
Mar 25, 2023Voluntary Action Indicated (VAI)No citations listed
Feb 22, 2018Voluntary Action Indicated (VAI)No citations listed
Dec 12, 2014No Action Indicated (NAI)No citations listed
Sep 13, 2012Voluntary Action Indicated (VAI)No citations listed
Feb 23, 2009Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Ethypharm
Location
Centre Val de Loire 28170 (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.