Patheon France S.A.S. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Patheon France S.A.S. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Patheon France S.A.S." is on file.

What these totals cover: FDA records filed under the name "Patheon France S.A.S." and its spelling variant "Patheon France". Records filed under related names are not included; see Related names.

Latest recall
Z-0211-2027 · Aug 14, 2026 · filed under Life Technologies Holdings
Latest inspection
Sep 29, 2023 · VAI

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

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
Inspections5Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

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

Patheon France S.A.S.: FDA inspections per year 2017: 0 inspections020172018: 1 inspections120182019: 1 inspections120192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 1 inspections120232024: 0 inspections020242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400000
202310000
202200000
202100000
202000000
201910000
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.

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Recent FDA inspections

5 inspections from Mar 28, 2014 to Sep 29, 2023.

DateSiteProductClassificationFEI
Sep 29, 2023Bourgoin Jallieu Cedex, FranceDrugsVoluntary Action Indicated (VAI)3004468553
Sep 27, 2019Bourgoin Jallieu Cedex, FranceDrugsVoluntary Action Indicated (VAI)3004468553
Jun 8, 2018Bourgoin Jallieu Cedex, FranceDrugsVoluntary Action Indicated (VAI)3004468553
Mar 11, 2016Bourgoin Jallieu Cedex, FranceDrugsVoluntary Action Indicated (VAI)3004468553
Mar 28, 2014Bourgoin Jallieu Cedex, FranceDevicesVoluntary Action Indicated (VAI)3004468553
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 3004468553Bourgoin Jallieu Cedex, France5Sep 29, 2023

Patheon France S.A.S. and the FDA: common questions

Has Patheon France S.A.S. received an FDA warning letter?

No FDA warning letter addressed to the name "Patheon France S.A.S." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Patheon France S.A.S. received an FDA Form 483?

FDA has not published a Form 483 for "Patheon France S.A.S." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Patheon France S.A.S.?

The most recent FDA inspection on file ended Sep 29, 2023 at Bourgoin Jallieu Cedex, France and was classified VAI. FDA has 5 inspections of Patheon France S.A.S. on file.

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