Indena SpA
FDA inspection history in Milano, Italy, 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 Milano, Italy.
Cited most
Across all Indena SpA observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Indena SpA file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Milano, Italy
One Form 483 · 2016 · 1 observation
Latest: Form 483, Jul 29, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-07-29 | 483 Form 483 | Milano, Italy | 1 | $99 |
Investigators on these documents
FEI number 1000280888 · most recent document Jul 29, 2016
About Indena SpA
How many FDA Form 483s has Indena SpA received?
FDA Intel has 1 Form 483 on file for Indena SpA; the most recent is dated Jul 29, 2016.
When was Indena SpA last inspected by FDA?
The most recent FDA inspection document on file for Indena SpA is a Form 483 dated Jul 29, 2016, for the site in Milano, Italy.
What did FDA cite at Indena SpA?
The regulations cited most in the observations on file for Indena SpA are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.