Vetter Pharma Fertigung GmbH & Co. KG
FDA inspection history in Langenargen, Germany, 2016 to 2024
- 2
- Form 483s
Every document, by year
- Form 483
2016: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Langenargen, Germany.
- 2016The longest 483 on file: 6 observations over 7 pages at Langenargen, Germany.
- 2024One Form 483, at Langenargen, Germany.
Cited most
Across all Vetter Pharma Fertigung GmbH & Co. KG observations on file
- 21 CFR 211.100(b)Written procedures; deviations2
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.192Production record review1
- 21 CFR 211.198(a)Complaint files1
The complete Vetter Pharma Fertigung GmbH & Co. KG file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Langenargen, Germany
Two Form 483s · 2016 to 2024 · 9 observations
Latest: Form 483, Apr 24, 2024 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-04-24 | 483 Form 483 | Langenargen, Germany | 3 | $99 |
| 2016-04-26 | 483 Form 483 | Langenargen, Germany | 6 | $99 |
Investigators on these documents
FEI number 3002808846 · most recent document Apr 24, 2024
About Vetter Pharma Fertigung GmbH & Co. KG
How many FDA Form 483s has Vetter Pharma Fertigung GmbH & Co. KG received?
FDA Intel has 2 Form 483s on file for Vetter Pharma Fertigung GmbH & Co. KG; the most recent is dated Apr 24, 2024.
When was Vetter Pharma Fertigung GmbH & Co. KG last inspected by FDA?
The most recent FDA inspection document on file for Vetter Pharma Fertigung GmbH & Co. KG is a Form 483 dated Apr 24, 2024, for the site in Langenargen, Germany.
What did FDA cite at Vetter Pharma Fertigung GmbH & Co. KG?
The regulations cited most in the observations on file for Vetter Pharma Fertigung GmbH & Co. KG are 21 CFR 211.100(b) (Written procedures; deviations), 2 times; 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time.