Mankind Pharma Limited
Mankind Pharma Limited appears in FDA public data with 0 recalls, 1 510(k) clearance, 4 FDA inspections, and 0 compliance actions on record. Its most recent FDA inspection ended on Apr 26, 2025 (Voluntary Action Indicated (VAI)). Its most recent 510(k) clearance was granted on Apr 10, 2024.
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Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 4
- Compliance Actions
- 0
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Apr 26, 2025 | Kotputli-Behror, India | Drugs | Voluntary Action Indicated (VAI) | 3014150265 |
| Apr 13, 2023 | Gurugram, India | Drugs | Voluntary Action Indicated (VAI) | 3013913573 |
| Feb 25, 2022 | Rampur Ghat, India | Drugs | Voluntary Action Indicated (VAI) | 3009083745 |
| Jan 11, 2019 | Rampur Ghat, India | Drugs | Voluntary Action Indicated (VAI) | 3009083745 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K232523 | Sodium Chloride Inhalation Solution, USP 0.9%, 3% & 7% | Apr 10, 2024 |