Rivopharm SA
FDA inspection history in MANNO, Switzerland, 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 MANNO, Switzerland.
Cited most
Across all Rivopharm observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
The complete Rivopharm file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
MANNO, Switzerland
One Form 483 · 2019 · 1 observation
Latest: Form 483, Jan 18, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-01-18 | 483 Form 483 | MANNO, Switzerland | 1 | $99 |
Investigators on these documents
FEI number 3005884589 · most recent document Jan 18, 2019
About Rivopharm SA
How many FDA Form 483s has Rivopharm SA received?
FDA Intel has 1 Form 483 on file for Rivopharm SA; the most recent is dated Jan 18, 2019.
When was Rivopharm SA last inspected by FDA?
The most recent FDA inspection document on file for Rivopharm SA is a Form 483 dated Jan 18, 2019, for the site in MANNO, Switzerland.
What did FDA cite at Rivopharm SA?
The regulations cited most in the observations on file for Rivopharm SA are 21 CFR 211.100(a) (Written procedures; deviations), 1 time.