Catalent Micron Technologies, Inc.
FDA Regulatory Profile
Catalent Micron Technologies, Inc. has 0 FDA recalls, 13 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Jun 9, 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 |
|---|
| Jun 9, 2025 | Malvern, PA | Drugs | Voluntary Action Indicated (VAI) | 3007992266 |
| Jun 22, 2022 | Dartford, United Kingdom | Drugs | Voluntary Action Indicated (VAI) | 3002807652 |
| Mar 21, 2019 | Malvern, PA | Drugs | No Action Indicated (NAI) | 3007992266 |
| May 3, 2017 | Dartford, United Kingdom | Drugs | Voluntary Action Indicated (VAI) | 3002807652 |
| Jan 19, 2017 | Dartford, United Kingdom | Drugs | Voluntary Action Indicated (VAI) | 3002807652 |
| Apr 20, 2016 | Malvern, PA | Drugs | Voluntary Action Indicated (VAI) | 3007992266 |
| Apr 11, 2014 | Dartford, United Kingdom | Drugs | No Action Indicated (NAI) | 3002807652 |
| Jun 12, 2013 | Malvern, PA | Drugs | No Action Indicated (NAI) | 3007992266 |
| Aug 25, 2011 | Dartford, United Kingdom | Drugs | No Action Indicated (NAI) | 3002807652 |
| Dec 8, 2010 | Malvern, PA | Drugs | Voluntary Action Indicated (VAI) | 3007992266 |
| Mar 31, 2010 | Malvern, PA | Drugs | No Action Indicated (NAI) | 3007992266 |
| Feb 23, 2010 | Malvern, PA | Drugs | No Action Indicated (NAI) | 3007992266 |
| Apr 8, 2009 | Dartford, United Kingdom | Drugs | Voluntary Action Indicated (VAI) | 3002807652 |
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.