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
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections8Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Catalent Pharma Solutions
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Catalent Cts
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Catalent Germany Eberbach
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Catalent Germany Schorndorf
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Catalent Micron Technologies
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Catalent France Beinheim
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Catalent Maryland
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Catalent Micron Technologies, Limited
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Catalent Massachusetts
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0030—

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 20, 2026Anagni, ItalyBiologicsNo Action Indicated (NAI)3002806546
Feb 23, 2024Anagni, ItalyDrugsVoluntary Action Indicated (VAI)3002806546
Feb 14, 2020Anagni, ItalyDrugsVoluntary Action Indicated (VAI)3002806546
Mar 31, 2017Anagni, ItalyDrugsVoluntary Action Indicated (VAI)3002806546
Nov 20, 2015Anagni, ItalyVeterinaryVoluntary Action Indicated (VAI)3002806546
Jul 2, 2013Anagni, ItalyDrugsVoluntary Action Indicated (VAI)3002806546
Mar 8, 2012Anagni, ItalyDrugsVoluntary Action Indicated (VAI)3002806546
Mar 15, 2011Anagni, ItalyDrugsVoluntary 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

FacilityLocationInspectionsLatest
FEI 3002806546Anagni, Italy8Jan 20, 2026

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.