Pajunk GmbH
FDA inspection history in Geisingen, Germany, 2004 to 2016
- 1
- Form 483
- 1
- Warning letter
Every document, by year
- Form 483
- Warning letter
2004: one warning letter; 2016: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2004One warning letter.
- 2016One Form 483, at Geisingen, Germany.
Cited most
Across all Pajunk observations on file
- 21 CFR 820.30Design controls1
- 21 CFR 820.50Purchasing controls1
- 21 CFR 820.70Production and process controls1
The complete Pajunk 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
Geisingen, Germany
One Form 483 · 2016 · 3 observations
Latest: Form 483, Feb 18, 2016 →
Also: one document not tied to a site.
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-02-18 | 483 Form 483 | Geisingen, Germany | 3 | $99 |
| 2004-11-17 | Warning letter Warning letter | — | — | $99 |
Investigators on these documents
FEI number 3002807847 · most recent document Feb 18, 2016
About Pajunk GmbH
How many FDA Form 483s has Pajunk GmbH received?
FDA Intel has 1 Form 483 on file for Pajunk GmbH; the most recent is dated Feb 18, 2016.
When was Pajunk GmbH last inspected by FDA?
The most recent FDA inspection document on file for Pajunk GmbH is a Form 483 dated Feb 18, 2016, for the site in Geisingen, Germany.
What did FDA cite at Pajunk GmbH?
The regulations cited most in the observations on file for Pajunk GmbH are 21 CFR 820.30 (Design controls), 1 time; 21 CFR 820.50 (Purchasing controls), 1 time; 21 CFR 820.70 (Production and process controls), 1 time.
Has Pajunk GmbH received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Pajunk GmbH; the most recent is dated Nov 17, 2004.