FEI 3017734754
FDA inspection history in ALCALA DE HENARES, Spain, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at ALCALA DE HENARES, Spain.
Cited most
Across all site observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.122Materials examination and usage criteria1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
ALCALA DE HENARES, Spain
One Form 483 · 2024 · 11 observations
Latest: Form 483, Apr 16, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-04-16 | 483 Form 483 | ALCALA DE HENARES, Spain | 11 | $99 |
Investigators on these documents
Marcus A. Ray (1)Ofthis Marcus A. Ray (1)Pratik S. Upadhyay (1)
FEI number 3017734754 · most recent document Apr 16, 2024
About FEI 3017734754
How many FDA Form 483s has FEI 3017734754 received?
FDA Intel has 1 Form 483 on file for FEI 3017734754; the most recent is dated Apr 16, 2024.
When was FEI 3017734754 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3017734754 is a Form 483 dated Apr 16, 2024, for the site in ALCALA DE HENARES, Spain.
What did FDA cite at FEI 3017734754?
The regulations cited most in the observations on file for FEI 3017734754 are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time.