Catalent Greenville Inc
FDA Regulatory Profile
Catalent Greenville Inc has 0 FDA recalls, 13 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Oct 24, 2025 · VAI
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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 | 13 | Nov 8, 2026 | Newest record Oct 28, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|
| Oct 24, 2025 | Greenville, NC | Drugs | Voluntary Action Indicated (VAI) | 3000209735 |
| Jan 31, 2024 | Greenville, NC | Drugs | No Action Indicated (NAI) | 3000209735 |
| Jul 12, 2019 | Greenville, NC | Drugs | Voluntary Action Indicated (VAI) | 3000209735 |
| Aug 24, 2018 | Greenville, NC | Drugs | No Action Indicated (NAI) | 3000209735 |
| Apr 13, 2017 | Greenville, NC | Drugs | No Action Indicated (NAI) | 3000209735 |
| Jul 14, 2016 | Greenville, NC | Drugs | No Action Indicated (NAI) | 3000209735 |
| May 2, 2014 | Greenville, NC | Drugs | No Action Indicated (NAI) | 3000209735 |
| Aug 21, 2013 | Greenville, NC | Drugs | No Action Indicated (NAI) | 3000209735 |
| May 11, 2012 | Greenville, NC | Drugs | Voluntary Action Indicated (VAI) | 3000209735 |
| May 11, 2012 | Greenville, NC | Drugs | Voluntary Action Indicated (VAI) | 3000209735 |
| Mar 18, 2011 | Greenville, NC | Drugs | Voluntary Action Indicated (VAI) | 3000209735 |
| Oct 1, 2010 | Greenville, NC | Drugs | Voluntary Action Indicated (VAI) | 3000209735 |
| Nov 13, 2009 | Greenville, NC | Drugs | No Action Indicated (NAI) | 3000209735 |
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 3000209735 | Greenville, NC | 13 | Oct 24, 2025 |