Fisiopharma SRL
FDA inspection history in Palomonte, Italy, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Palomonte, Italy.
Cited most
Across all Fisiopharma SRL observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.113(b)Control of microbiological contamination1
- 21 CFR 211.165(e)Testing and release for distribution1
- 21 CFR 211.180(e)(2)General requirements1
- 21 CFR 211.186(b)(9)Master production and control records1
The complete Fisiopharma SRL file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Palomonte, Italy
One Form 483 · 2019 · 10 observations
Latest: Form 483, Sep 27, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-09-27 | 483 Form 483 | Palomonte, Italy | 10 | $99 |
FEI number 3006435023 · most recent document Sep 27, 2019
About Fisiopharma SRL
How many FDA Form 483s has Fisiopharma SRL received?
FDA Intel has 1 Form 483 on file for Fisiopharma SRL; the most recent is dated Sep 27, 2019.
When was Fisiopharma SRL last inspected by FDA?
The most recent FDA inspection document on file for Fisiopharma SRL is a Form 483 dated Sep 27, 2019, for the site in Palomonte, Italy.
What did FDA cite at Fisiopharma SRL?
The regulations cited most in the observations on file for Fisiopharma SRL are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.113(b) (Control of microbiological contamination), 1 time; 21 CFR 211.165(e) (Testing and release for distribution), 1 time.