Catalent France Beinheim SA FDA Inspection Record

FEI 3002808036 · Inspections, Form 483s, warning letters and import refusals

Catalent France Beinheim SA is an FDA-registered facility (FEI 3002808036) located in 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 25, 2022: Voluntary Action Indicated (VAI)
Inspections on record
6 (4 VAI, 2 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
10 or more

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 25, 2022Voluntary Action Indicated (VAI)No citations listed
Oct 29, 2020Voluntary Action Indicated (VAI)No citations listed
Jul 21, 2017Voluntary Action Indicated (VAI)No citations listed
Mar 20, 2014No Action Indicated (NAI)No citations listed
Jul 13, 2012No Action Indicated (NAI)No citations listed
Sep 17, 2009Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Catalent France Beinheim SA
Location
FR
Registration Expires
Dec 31, 2027
Operations
ANALYSIS; MANUFACTURE
Source
decrs

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