Italfarmaco S.A.
FDA inspection history in Alcobendas, Spain, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Alcobendas, Spain.
Cited most
Across all Italfarmaco observations on file
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Italfarmaco file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Alcobendas, Spain
One Form 483 · 2023 · 1 observation
Latest: Form 483, Sep 15, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-09-15 | 483 Form 483 | Alcobendas, Spain | 1 | $99 |
Investigators on these documents
FEI number 3007048260 · most recent document Sep 15, 2023
About Italfarmaco S.A.
How many FDA Form 483s has Italfarmaco S.A. received?
FDA Intel has 1 Form 483 on file for Italfarmaco S.A.; the most recent is dated Sep 15, 2023.
When was Italfarmaco S.A. last inspected by FDA?
The most recent FDA inspection document on file for Italfarmaco S.A. is a Form 483 dated Sep 15, 2023, for the site in Alcobendas, Spain.
What did FDA cite at Italfarmaco S.A.?
The regulations cited most in the observations on file for Italfarmaco S.A. are 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.