Merz Pharma GmbH & Co. KGaA FDA Inspection Record

FEI 3006999111 · Inspections, Form 483s, warning letters and import refusals

Merz Pharma GmbH & Co. KGaA is an FDA-registered facility (FEI 3006999111) located in Reinheim Hesse, DE. Registered operations: LABEL; MANUFACTURE; PACK. RegDataLab tracks 3 FDA inspections at this facility.

Reviewing Merz Pharma GmbH & Co. KGaA as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Merz Pharma GmbH & Co. KGaA yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

What FDA found at this site

Latest inspection
Nov 6, 2024: Voluntary Action Indicated (VAI)
Inspections on record
3 (2 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
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 6, 2024Voluntary Action Indicated (VAI)No citations listed
Aug 23, 2019Voluntary Action Indicated (VAI)No citations listed
Apr 29, 2016No Action Indicated (NAI)No citations listed

Facility details

Company
Merz Pharma Gmbh & Co. KGaA
Location
Reinheim Hesse (DE)
Registration Expires
Dec 31, 2026
Operations
LABEL; MANUFACTURE; PACK
Source
both

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