Catalent Anagni SRL
FDA Regulatory Profile
Catalent Anagni SRL has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Jan 20, 2026 · NAI
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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 | 8 | 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 |
| Jan 20, 2026 | Anagni, Italy | Biologics | No Action Indicated (NAI) | 3002806546 |
| Feb 23, 2024 | Anagni, Italy | Drugs | Voluntary Action Indicated (VAI) | 3002806546 |
| Feb 14, 2020 | Anagni, Italy | Drugs | Voluntary Action Indicated (VAI) | 3002806546 |
| Mar 31, 2017 | Anagni, Italy | Drugs | Voluntary Action Indicated (VAI) | 3002806546 |
| Nov 20, 2015 | Anagni, Italy | Veterinary | Voluntary Action Indicated (VAI) | 3002806546 |
| Jul 2, 2013 | Anagni, Italy | Drugs | Voluntary Action Indicated (VAI) | 3002806546 |
| Mar 8, 2012 | Anagni, Italy | Drugs | Voluntary Action Indicated (VAI) | 3002806546 |
| Mar 15, 2011 | Anagni, Italy | Drugs | Voluntary Action Indicated (VAI) | 3002806546 |
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 3002806546 | Anagni, Italy | 8 | Jan 20, 2026 |