Mentha & Allied Products Private Ltd. FDA Record
Mentha & Allied Products Private Ltd. has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Mentha & Allied Products Private Ltd., the most recent on Apr 16, 2025.
- Latest inspection
- Sep 25, 2024 · OAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 2 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 1 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
FDA record by year
| Year | Inspections | OAI | Warning letters | Recall records | Class I |
|---|---|---|---|---|---|
| 2026 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 1 | 0 | 0 |
| 2024 | 1 | 1 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2017 | 1 | 1 | 0 | 0 | 0 |
Reviewing Mentha & Allied Products Private Ltd. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Or check Mentha & Allied Products Private Ltd. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.
Mentha & Allied Products Private Ltd. FDA Warning Letters
| Issued | Subject | Issuing office | Close-out letter |
|---|---|---|---|
| Apr 16, 2025 · Letter on fda.gov | CGMP/Active Pharmaceutical Ingredient (API)/Adulterated | Center for Drug Evaluation and Research (CDER) |
Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Sep 25, 2024 | Rampur, India | Drugs | Official Action Indicated (OAI) | 3004293613 |
| Sep 8, 2017 | Rampur, India | Drugs | Official Action Indicated (OAI) | 3004293613 |
- NAI
- No objectionable conditions or practices were found during the inspection.
- VAI
- Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
- OAI
- Regulatory and/or administrative actions are recommended.
Compliance Actions
FDA's compliance actions data lists 1 compliance action under Mentha & Allied Products Private Ltd.: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3004293613 | Rampur, India | 2 | Sep 25, 2024 |
Mentha & Allied Products Private Ltd. and the FDA: common questions
Has Mentha & Allied Products Private Ltd. received an FDA warning letter?
Yes. FDA has issued 1 warning letter to Mentha & Allied Products Private Ltd.. The most recent is dated Apr 16, 2025, with the subject "CGMP/Active Pharmaceutical Ingredient (API)/Adulterated".
Has Mentha & Allied Products Private Ltd. received an FDA Form 483?
FDA has not published a Form 483 for "Mentha & Allied Products Private Ltd." in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Mentha & Allied Products Private Ltd.?
The most recent FDA inspection on file ended Sep 25, 2024 at Rampur, India and was classified OAI. FDA has 2 inspections of Mentha & Allied Products Private Ltd. on file, 2 of them classified OAI (official action indicated).
Need more than this page shows? Ask about Mentha & Allied Products Private Ltd. in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.