Corden Pharma GmbH — FDA Facility Profile

FEI 3007014398

Corden Pharma GmbH is an FDA-registered facility (FEI 3007014398) located in Germany, DE. Registered operations: ANALYSIS; LABEL; MANUFACTURE; PACK. RegDataLab tracks 5 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Oct 15, 2025: Voluntary Action Indicated (VAI)
Inspections on record
5 (2 VAI, 3 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
3

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 15, 2025Voluntary Action Indicated (VAI)No citations listed
Sep 14, 2022Voluntary Action Indicated (VAI)No citations listed
Jul 6, 2018No Action Indicated (NAI)No citations listed
Oct 24, 2014No Action Indicated (NAI)No citations listed
Nov 17, 2009No Action Indicated (NAI)No citations listed

Facility details

Company
Corden Pharma GmbH
Location
Germany (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.