Eurofarma Laboratorios S/A
FDA inspection history in Itapevi, Brazil, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Itapevi, Brazil.
Cited most
Across all Eurofarma Laboratorios S/A observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.194Laboratory records1
- 21 CFR 211.42Design and construction features1
- 21 CFR 211.46Ventilation, air filtration, air heating and cooling1
- 21 CFR 211.63Equipment design, size, and location1
The complete Eurofarma Laboratorios S/A file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Itapevi, Brazil
One Form 483 · 2022 · 5 observations
Latest: Form 483, Sep 20, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-09-20 | 483 Form 483 | Itapevi, Brazil | 5 | $99 |
Investigators on these documents
FEI number 3009538725 · most recent document Sep 20, 2022
About Eurofarma Laboratorios S/A
How many FDA Form 483s has Eurofarma Laboratorios S/A received?
FDA Intel has 1 Form 483 on file for Eurofarma Laboratorios S/A; the most recent is dated Sep 20, 2022.
When was Eurofarma Laboratorios S/A last inspected by FDA?
The most recent FDA inspection document on file for Eurofarma Laboratorios S/A is a Form 483 dated Sep 20, 2022, for the site in Itapevi, Brazil.
What did FDA cite at Eurofarma Laboratorios S/A?
The regulations cited most in the observations on file for Eurofarma Laboratorios S/A are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.194 (Laboratory records), 1 time; 21 CFR 211.42 (Design and construction features), 1 time.