Laboratorio Reig Jofre, S.A.
FDA inspection history in Barcelona, 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 Barcelona, Spain.
Cited most
Across all Laboratorio Reig Jofre observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.160General requirements1
- 21 CFR 211.167Special testing requirements1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Laboratorio Reig Jofre file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Barcelona, Spain
One Form 483 · 2019 · 8 observations
Latest: Form 483, Apr 5, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-04-05 | 483 Form 483 | Barcelona, Spain | 8 | $99 |
Investigators on these documents
FEI number 3003768199 · most recent document Apr 5, 2019
About Laboratorio Reig Jofre, S.A.
How many FDA Form 483s has Laboratorio Reig Jofre, S.A. received?
FDA Intel has 1 Form 483 on file for Laboratorio Reig Jofre, S.A.; the most recent is dated Apr 5, 2019.
When was Laboratorio Reig Jofre, S.A. last inspected by FDA?
The most recent FDA inspection document on file for Laboratorio Reig Jofre, S.A. is a Form 483 dated Apr 5, 2019, for the site in Barcelona, Spain.
What did FDA cite at Laboratorio Reig Jofre, S.A.?
The regulations cited most in the observations on file for Laboratorio Reig Jofre, S.A. are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.160 (General requirements), 1 time.