PharmaZell GmbH
FDA inspection history in Raubling, Germany, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Raubling, Germany.
Cited most
Across all PharmaZell observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.166Stability testing1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete PharmaZell file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Raubling, Germany
One Form 483 · 2017 · 3 observations
Latest: Form 483, Sep 22, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-09-22 | 483 Form 483 | Raubling, Germany | 3 | $99 |
Investigators on these documents
FEI number 3003725792 · most recent document Sep 22, 2017
About PharmaZell GmbH
How many FDA Form 483s has PharmaZell GmbH received?
FDA Intel has 1 Form 483 on file for PharmaZell GmbH; the most recent is dated Sep 22, 2017.
When was PharmaZell GmbH last inspected by FDA?
The most recent FDA inspection document on file for PharmaZell GmbH is a Form 483 dated Sep 22, 2017, for the site in Raubling, Germany.
What did FDA cite at PharmaZell GmbH?
The regulations cited most in the observations on file for PharmaZell GmbH are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.166 (Stability testing), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.