Instituto Grifols, S.A.
FDA inspection history in Parets Del Valles, 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 Parets Del Valles, Spain.
Cited most
Across all Instituto Grifols observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 600.80Postmarketing reporting of adverse experiences1
The complete Instituto Grifols file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Parets Del Valles, Spain
One Form 483 · 2019 · 2 observations
Latest: Form 483, Jun 25, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-06-25 | 483 Form 483 | Parets Del Valles, Spain | 2 | $99 |
Investigators on these documents
FEI number 3002807257 · most recent document Jun 25, 2019
About Instituto Grifols, S.A.
How many FDA Form 483s has Instituto Grifols, S.A. received?
FDA Intel has 1 Form 483 on file for Instituto Grifols, S.A.; the most recent is dated Jun 25, 2019.
When was Instituto Grifols, S.A. last inspected by FDA?
The most recent FDA inspection document on file for Instituto Grifols, S.A. is a Form 483 dated Jun 25, 2019, for the site in Parets Del Valles, Spain.
What did FDA cite at Instituto Grifols, S.A.?
The regulations cited most in the observations on file for Instituto Grifols, S.A. are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 600.80 (Postmarketing reporting of adverse experiences), 1 time.