Laboratorios Leon Farma SAU
FDA inspection history in VILLAQUILAMBRE, Spain, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at VILLAQUILAMBRE, Spain.
Cited most
Across all Laboratorios Leon Farma SAU observations on file
- 21 CFR 820.184Device history record2
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.100Corrective and preventive action1
- 21 CFR 820.198Complaint files1
- 21 CFR 820.50Purchasing controls1
The complete Laboratorios Leon Farma SAU file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
VILLAQUILAMBRE, Spain
One Form 483 · 2018 · 7 observations
Latest: Form 483, May 25, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-05-25 | 483 Form 483 | VILLAQUILAMBRE, Spain | 7 | $99 |
FEI number 3006188375 · most recent document May 25, 2018
About Laboratorios Leon Farma SAU
How many FDA Form 483s has Laboratorios Leon Farma SAU received?
FDA Intel has 1 Form 483 on file for Laboratorios Leon Farma SAU; the most recent is dated May 25, 2018.
When was Laboratorios Leon Farma SAU last inspected by FDA?
The most recent FDA inspection document on file for Laboratorios Leon Farma SAU is a Form 483 dated May 25, 2018, for the site in VILLAQUILAMBRE, Spain.
What did FDA cite at Laboratorios Leon Farma SAU?
The regulations cited most in the observations on file for Laboratorios Leon Farma SAU are 21 CFR 820.184 (Device history record), 2 times; 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 820.100 (Corrective and preventive action), 1 time.