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Vetter Pharma Fertigung GmbH & Co. KG (Langenargen Eisenbahnstrasse) — FDA Facility Profile

FEI 3002808846

Vetter Pharma Fertigung GmbH & Co. KG (Langenargen Eisenbahnstrasse) is an FDA-registered facility (FEI 3002808846) located in Baden-Wuerttemberg, DE. Registered operations: ANALYSIS; MANUFACTURE. RegDataLab tracks 9 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Mar 20, 2024: Voluntary Action Indicated (VAI)
Inspections on record
9 (5 VAI, 4 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
Mar 20, 2024Voluntary Action Indicated (VAI)No citations listed
May 24, 2022Voluntary Action Indicated (VAI)No citations listed
Sep 13, 2019No Action Indicated (NAI)No citations listed
Sep 21, 2018No Action Indicated (NAI)No citations listed
Nov 10, 2017Voluntary Action Indicated (VAI)No citations listed
Apr 26, 2016Voluntary Action Indicated (VAI)Procedures not in writing, fully followed (21 CFR 211.22(d))
Calibration/Inspection/Checking not done (21 CFR 211.68(a))
SOPs not followed / documented (21 CFR 211.100(b))
Investigations of discrepancies, failures (21 CFR 211.192)
and 2 more
Feb 20, 2014No Action Indicated (NAI)No citations listed
Jul 17, 2012No Action Indicated (NAI)No citations listed
Apr 1, 2010Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Vetter Pharma Fertigung GmbH & Co. KG (Langenargen Eisenbahnstrasse)
Location
Baden-Wuerttemberg (DE)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; MANUFACTURE
Source
decrs

FDA data resources

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