Ferring GmbH — FDA Facility Profile

FEI 3002806979

Ferring GmbH is an FDA-registered facility (FEI 3002806979) located in Kiel, DE. Registered operations: ANALYSIS; LABEL; MANUFACTURE; PACK. RegDataLab tracks 7 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Feb 29, 2024: Voluntary Action Indicated (VAI)
Inspections on record
7 (7 VAI)
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
Feb 29, 2024Voluntary Action Indicated (VAI)No citations listed
Sep 30, 2021Voluntary Action Indicated (VAI)No citations listed
Aug 23, 2019Voluntary Action Indicated (VAI)Test methods (21 CFR 211.165(e))
Jan 27, 2017Voluntary Action Indicated (VAI)No citations listed
Nov 11, 2014Voluntary Action Indicated (VAI)No citations listed
Oct 26, 2012Voluntary Action Indicated (VAI)Training , Education , Experience overall (21 CFR 211.25(a))
Procedures for sterile drug products (21 CFR 211.113(b))
Establish reliability of supplier's C of A (21 CFR 211.84(d)(3))
Investigations of discrepancies, failures (21 CFR 211.192)
and 2 more
Nov 19, 2010Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Ferring GmbH
Location
Kiel (DE)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; LABEL; MANUFACTURE; PACK
Source
decrs

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