Mipharm SPA
FDA inspection history in MILANO, Italy, 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 MILANO, Italy.
Cited most
Across all Mipharm SPA observations on file
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.166Stability testing1
- 21 CFR 211.192Production record review1
The complete Mipharm SPA file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
MILANO, Italy
One Form 483 · 2023 · 3 observations
Latest: Form 483, Sep 22, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-09-22 | 483 Form 483 | MILANO, Italy | 3 | $99 |
Investigators on these documents
FEI number 3002807647 · most recent document Sep 22, 2023
About Mipharm SPA
How many FDA Form 483s has Mipharm SPA received?
FDA Intel has 1 Form 483 on file for Mipharm SPA; the most recent is dated Sep 22, 2023.
When was Mipharm SPA last inspected by FDA?
The most recent FDA inspection document on file for Mipharm SPA is a Form 483 dated Sep 22, 2023, for the site in MILANO, Italy.
What did FDA cite at Mipharm SPA?
The regulations cited most in the observations on file for Mipharm SPA are 21 CFR 211.165 (Testing and release for distribution), 1 time; 21 CFR 211.166 (Stability testing), 1 time; 21 CFR 211.192 (Production record review), 1 time.