FEI 1000183111
FDA inspection history in Mexico City, Mexico, 2019 to 2022
- 2
- Form 483s
Every document, by year
- Form 483
2019: one Form 483; 2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Mexico City, Mexico.
- 2019The longest 483 on file: 3 observations over 3 pages at Mexico City, Mexico.
- 2022One Form 483, at Mexico City, Mexico.
Cited most
Across all site observations on file
- 21 CFR 211.166Stability testing1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(c)Responsibilities of quality control unit1
- 21 CFR 211.48(a)Plumbing1
- 21 CFR 211.63Equipment design, size, and location1
The complete site file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Mexico City, Mexico
Two Form 483s · 2019 to 2022 · 6 observations
Latest: Form 483, May 20, 2022 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-05-20 | 483 Form 483 | Mexico City, Mexico | 3 | $99 |
| 2019-12-06 | 483 Form 483 | Mexico City, Mexico | 3 | $99 |
Investigators on these documents
FEI number 1000183111 · most recent document May 20, 2022
About FEI 1000183111
How many FDA Form 483s has FEI 1000183111 received?
FDA Intel has 2 Form 483s on file for FEI 1000183111; the most recent is dated May 20, 2022.
When was FEI 1000183111 last inspected by FDA?
The most recent FDA inspection document on file for FEI 1000183111 is a Form 483 dated May 20, 2022, for the site in Mexico City, Mexico.
What did FDA cite at FEI 1000183111?
The regulations cited most in the observations on file for FEI 1000183111 are 21 CFR 211.166 (Stability testing), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22(c) (Responsibilities of quality control unit), 1 time.