FEI 3007102377
FDA inspection history in Zapopan, Mexico, 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 Zapopan, Mexico.
Cited most
Across all site observations on file
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.170Reserve samples1
- 21 CFR 211.192Production record review1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Zapopan, Mexico
One Form 483 · 2018 · 4 observations
Latest: Form 483, Dec 4, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-12-04 | 483 Form 483 | Zapopan, Mexico | 4 | $99 |
Investigators on these documents
FEI number 3007102377 · most recent document Dec 4, 2018
About FEI 3007102377
How many FDA Form 483s has FEI 3007102377 received?
FDA Intel has 1 Form 483 on file for FEI 3007102377; the most recent is dated Dec 4, 2018.
When was FEI 3007102377 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3007102377 is a Form 483 dated Dec 4, 2018, for the site in Zapopan, Mexico.
What did FDA cite at FEI 3007102377?
The regulations cited most in the observations on file for FEI 3007102377 are 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.170 (Reserve samples), 1 time; 21 CFR 211.192 (Production record review), 1 time.