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Patheon UK Limited

FDA Regulatory Profile

Patheon UK Limited has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Patheon UK Limited". Records filed under related names are not included; see Related names.

Latest inspection
Jul 7, 2026 · VAI

Newer recall under related name Life Technologies Holdings: Aug 14, 2026, Z-0211-2027.

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections8Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Patheon UK Limited's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Patheon UK Limited: FDA inspections per year 2017: 0 inspections020172018: 1 inspections120182019: 0 inspections020192020: 0 inspections020202021: 1 inspections120212022: 0 inspections020222023: 0 inspections020232024: 0 inspections020242025: 0 inspections020252026: 1 inspections12026
YearInspectionsOAIWarning lettersRecall recordsClass I
202610000
202500000
202400000
202300000
202200000
202110000
202000000
201900000
201810000
201700000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA inspections

8 inspections from Dec 9, 2008 to Jul 7, 2026.

DateSiteProductClassificationFEI
Jul 7, 2026Swindon, United KingdomDrugsVoluntary Action Indicated (VAI)3002807216
Sep 17, 2021Swindon, United KingdomDrugsVoluntary Action Indicated (VAI)3002807216
Mar 1, 2018Swindon, United KingdomDrugsVoluntary Action Indicated (VAI)3002807216
May 8, 2015Swindon, United KingdomDrugsVoluntary Action Indicated (VAI)3002807216
Sep 12, 2014Swindon, United KingdomDrugsVoluntary Action Indicated (VAI)3002807216
Jul 20, 2012Swindon, United KingdomDrugsVoluntary Action Indicated (VAI)3002807216
Jun 24, 2009Swindon, United KingdomDrugsVoluntary Action Indicated (VAI)3002807216
Dec 9, 2008Swindon, United KingdomDrugsVoluntary Action Indicated (VAI)3002807216
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3002807216Swindon, United Kingdom8Jul 7, 2026

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FDA data resources

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