Celgene Chemicals, GmbH
FDA inspection history in Zofingen, Switzerland, 2016
- 1
- Form 483
Every document, by year
- Form 483
2016: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Zofingen, Switzerland.
Cited most
Across all Celgene Chemicals observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Celgene Chemicals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Zofingen, Switzerland
One Form 483 · 2016 · 3 observations
Latest: Form 483, Jan 29, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-01-29 | 483 Form 483 | Zofingen, Switzerland | 3 | $99 |
Investigators on these documents
FEI number 3006305265 · most recent document Jan 29, 2016
About Celgene Chemicals, GmbH
How many FDA Form 483s has Celgene Chemicals, GmbH received?
FDA Intel has 1 Form 483 on file for Celgene Chemicals, GmbH; the most recent is dated Jan 29, 2016.
When was Celgene Chemicals, GmbH last inspected by FDA?
The most recent FDA inspection document on file for Celgene Chemicals, GmbH is a Form 483 dated Jan 29, 2016, for the site in Zofingen, Switzerland.
What did FDA cite at Celgene Chemicals, GmbH?
The regulations cited most in the observations on file for Celgene Chemicals, GmbH are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time.