Apotex Pharmachem India Pvt Ltd. FDA Record
Apotex Pharmachem India Pvt Ltd. has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Apotex Pharmachem India Pvt Ltd., the most recent on Jun 16, 2014.
- Latest inspection
- Mar 14, 2025 · VAI
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 | 7 | 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 | 1 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 1 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 1 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 1 | 0 | 0 | 0 | 0 |
| 2017 | 0 | 0 | 0 | 0 | 0 |
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Apotex Pharmachem India Pvt Ltd. FDA Warning Letters
| Issued | Subject | Issuing office | Close-out letter |
|---|---|---|---|
| Jun 16, 2014 |
Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Mar 14, 2025 | Bangalore, India | Drugs | Voluntary Action Indicated (VAI) | 3005466325 |
| Sep 2, 2022 | Bangalore, India | Drugs | No Action Indicated (NAI) | 3005466325 |
| Jan 31, 2020 | Bangalore, India | Drugs | Voluntary Action Indicated (VAI) | 3005466325 |
| Jun 26, 2018 | Bangalore, India | Drugs | Voluntary Action Indicated (VAI) | 3005466325 |
| Jun 3, 2016 | Bangalore, India | Drugs | Voluntary Action Indicated (VAI) | 3005466325 |
| Jan 31, 2014 | Bangalore, India | Drugs | Official Action Indicated (OAI) | 3005466325 |
| Dec 1, 2010 | Bangalore, India | Drugs | Voluntary Action Indicated (VAI) | 3005466325 |
- 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 Apotex Pharmachem India Pvt Ltd.: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3005466325 | Bangalore, India | 7 | Mar 14, 2025 |
Apotex Pharmachem India Pvt Ltd. and the FDA: common questions
Has Apotex Pharmachem India Pvt Ltd. received an FDA warning letter?
Yes. FDA has issued 1 warning letter to Apotex Pharmachem India Pvt Ltd.. The most recent is dated Jun 16, 2014.
Has Apotex Pharmachem India Pvt Ltd. received an FDA Form 483?
FDA has not published a Form 483 for "Apotex Pharmachem India Pvt Ltd." in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Apotex Pharmachem India Pvt Ltd.?
The most recent FDA inspection on file ended Mar 14, 2025 at Bangalore, India and was classified VAI. FDA has 7 inspections of Apotex Pharmachem India Pvt Ltd. on file, 1 of them classified OAI (official action indicated).
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