Laboratorios Farmalan, S.A.
FDA inspection history in VILLAQUILAMBRE, Spain, 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 VILLAQUILAMBRE, Spain.
Cited most
Across all Laboratorios Farmalan observations on file
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.42Design and construction features1
- 21 CFR 211.46Ventilation, air filtration, air heating and cooling1
The complete Laboratorios Farmalan file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
VILLAQUILAMBRE, Spain
One Form 483 · 2019 · 5 observations
Latest: Form 483, Mar 19, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-03-19 | 483 Form 483 | VILLAQUILAMBRE, Spain | 5 | $99 |
Investigators on these documents
FEI number 3014424887 · most recent document Mar 19, 2019
About Laboratorios Farmalan, S.A.
How many FDA Form 483s has Laboratorios Farmalan, S.A. received?
FDA Intel has 1 Form 483 on file for Laboratorios Farmalan, S.A.; the most recent is dated Mar 19, 2019.
When was Laboratorios Farmalan, S.A. last inspected by FDA?
The most recent FDA inspection document on file for Laboratorios Farmalan, S.A. is a Form 483 dated Mar 19, 2019, for the site in VILLAQUILAMBRE, Spain.
What did FDA cite at Laboratorios Farmalan, S.A.?
The regulations cited most in the observations on file for Laboratorios Farmalan, S.A. are 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.