Corden Pharma Bergamo SpA
FDA inspection history in Treviglio, Italy, 2016 to 2018
- 2
- Form 483s
Every document, by year
- Form 483
2016: one Form 483; 2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016–18Two Form 483s, at Treviglio, Italy.
- 2018The longest 483 on file: 7 observations over 2 pages at Treviglio, Italy.
Cited most
Across all Corden Pharma Bergamo SpA observations on file
- 21 CFR 211.198Complaint files2
- 21 CFR 211.67Equipment cleaning and maintenance2
- 21 CFR 211.111Time limitations on production1
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.188Batch production and control records1
The complete Corden Pharma Bergamo SpA 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
Treviglio, Italy
Two Form 483s · 2016 to 2018 · 11 observations
Latest: Form 483, Sep 27, 2018 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-09-27 | 483 Form 483 | Treviglio, Italy | 7 | $99 |
| 2016-06-17 | 483 Form 483 | Treviglio, Italy | 4 | $99 |
FEI number 3002806963 · most recent document Sep 27, 2018
About Corden Pharma Bergamo SpA
How many FDA Form 483s has Corden Pharma Bergamo SpA received?
FDA Intel has 2 Form 483s on file for Corden Pharma Bergamo SpA; the most recent is dated Sep 27, 2018.
When was Corden Pharma Bergamo SpA last inspected by FDA?
The most recent FDA inspection document on file for Corden Pharma Bergamo SpA is a Form 483 dated Sep 27, 2018, for the site in Treviglio, Italy.
What did FDA cite at Corden Pharma Bergamo SpA?
The regulations cited most in the observations on file for Corden Pharma Bergamo SpA are 21 CFR 211.198 (Complaint files), 2 times; 21 CFR 211.67 (Equipment cleaning and maintenance), 2 times; 21 CFR 211.111 (Time limitations on production), 1 time.