Medinatura New Mexico Inc.
FDA inspection history in Albuquerque, New Mexico, 2019 to 2025
- 1
- Warning letter
- 1
- Form 483
Every document, by year
- Warning letter
- Form 483
2019: one Form 483; 2025: one warning letter.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Albuquerque, New Mexico.
- 2025One warning letter, at Albuquerque, New Mexico.
Cited most
Across all Medinatura New Mexico observations on file
- 21 CFR 211.160General requirements3
- 21 CFR 211.188Batch production and control records2
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures2
- 21 CFR 211.184Component, drug product container, closure, and labeling records1
- 21 CFR 211.192Production record review1
The complete Medinatura New Mexico 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
Albuquerque, New Mexico
One warning letter and one Form 483 · 2019 to 2025 · 10 observations
Latest: Warning letter, Dec 10, 2025 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-12-10 | Warning letter Warning letter | Albuquerque, New Mexico | — | $99 |
| 2019-12-18 | 483 Form 483 | Albuquerque, New Mexico | 10 | $99 |
FEI number 1626962 · most recent document Dec 10, 2025
About Medinatura New Mexico Inc.
How many FDA Form 483s has Medinatura New Mexico Inc. received?
FDA Intel has 1 Form 483 on file for Medinatura New Mexico Inc.; the most recent is dated Dec 18, 2019.
When was Medinatura New Mexico Inc. last inspected by FDA?
The most recent FDA inspection document on file for Medinatura New Mexico Inc. is a Form 483 dated Dec 18, 2019, for the site in Albuquerque, New Mexico.
What did FDA cite at Medinatura New Mexico Inc.?
The regulations cited most in the observations on file for Medinatura New Mexico Inc. are 21 CFR 211.160 (General requirements), 3 times; 21 CFR 211.188 (Batch production and control records), 2 times; 21 CFR 211.84 (Testing and approval or rejection of components, drug product containers, and closures), 2 times.
Has Medinatura New Mexico Inc. received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Medinatura New Mexico Inc.; the most recent is dated Dec 10, 2025.