Raptim Research Pvt. Ltd.
FDA Regulatory Profile
Raptim Research Pvt. Ltd. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Jul 25, 2025 · OAI
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Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
|---|
| Recalls | 0 | Nov 4, 2026 (checked Nov 8, 2026, unchanged) | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 6 | Nov 8, 2026 | Newest record Oct 28, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Related names
| Name | Recalls | 510(k) | Inspections | Compliance | Most recent recall |
|---|
Raptim Research
Same company group | 0 | 0 | 1 | 0 | — |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|
| Jul 25, 2025 | Navi Mumbai, India | Drugs | Official Action Indicated (OAI) | 3007267856 |
| Apr 28, 2023 | Navi Mumbai, India | Drugs | Official Action Indicated (OAI) | 3007267856 |
| Sep 14, 2022 | Navi Mumbai, India | Drugs | No Action Indicated (NAI) | 3007267856 |
| Sep 19, 2019 | Navi Mumbai, India | Drugs | No Action Indicated (NAI) | 3007267856 |
| May 29, 2019 | Navi Mumbai, India | Drugs | No Action Indicated (NAI) | 3007267856 |
| Mar 22, 2019 | Navi Mumbai, India | Drugs | Voluntary Action Indicated (VAI) | 3007267856 |
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|
| FEI 3007267856 | Navi Mumbai, India | 6 | Jul 25, 2025 |