MENTHA AND ALLIED PRODUCTS PRIVATE LIMITED
FDA inspection history in Rampur, India, 2024 to 2025
- 1
- Warning letter
- 1
- Form 483
Every document, by year
- Warning letter
- Form 483
2024: one Form 483; 2025: one warning letter.
The story so far
Built from the dates and citations on the documents themselves.
- 2024–25One Form 483 and one warning letter, at Rampur, India.
Cited most
Across all MENTHA AND ALLIED PRODUCTS PRIVATE LIMITED observations on file
- 21 CFR 211.160General requirements3
- 21 CFR 211.188Batch production and control records2
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.80General requirements2
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures2
The complete MENTHA AND ALLIED PRODUCTS PRIVATE LIMITED 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
Rampur, India
One warning letter and one Form 483 · 2024 to 2025
Latest: Warning letter, Apr 16, 2025 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-04-16 | Warning letter Warning letter | Rampur, India | — | $99 |
| 2024-09-25 | 483 Form 483 | Rampur, India | — | $99 |
FEI number 3004293613 · most recent document Apr 16, 2025
About MENTHA AND ALLIED PRODUCTS PRIVATE LIMITED
How many FDA Form 483s has MENTHA AND ALLIED PRODUCTS PRIVATE LIMITED received?
FDA Intel has 1 Form 483 on file for MENTHA AND ALLIED PRODUCTS PRIVATE LIMITED; the most recent is dated Sep 25, 2024.
When was MENTHA AND ALLIED PRODUCTS PRIVATE LIMITED last inspected by FDA?
The most recent FDA inspection document on file for MENTHA AND ALLIED PRODUCTS PRIVATE LIMITED is a Form 483 dated Sep 25, 2024, for the site in Rampur, India.
What did FDA cite at MENTHA AND ALLIED PRODUCTS PRIVATE LIMITED?
The regulations cited most in the observations on file for MENTHA AND ALLIED PRODUCTS PRIVATE LIMITED are 21 CFR 211.160 (General requirements), 3 times; 21 CFR 211.188 (Batch production and control records), 2 times; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times.
Has MENTHA AND ALLIED PRODUCTS PRIVATE LIMITED received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for MENTHA AND ALLIED PRODUCTS PRIVATE LIMITED; the most recent is dated Apr 16, 2025.