Becton Dickinson France SAS FDA Record

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

Becton Dickinson France SAS has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Becton Dickinson France SAS" is on file.

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

Latest recall
Z-3275-2026 · Aug 20, 2026 · filed under Bard Peripheral Vascular
Latest inspection
Jan 25, 2013 · VAI

Newer recall under related name Bard Peripheral Vascular: Aug 20, 2026, Z-3275-2026.

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
Inspections2Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent FDA inspections

2 inspections from Jul 2, 2010 to Jan 25, 2013.

DateSiteProductClassificationFEI
Jan 25, 2013Le Pont-De-Claix, FranceDrugsVoluntary Action Indicated (VAI)1000173750
Jul 2, 2010Le Pont-De-Claix, FranceDrugsNo Action Indicated (NAI)1000173750
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 1000173750Le Pont-De-Claix, France2Jan 25, 2013

Becton Dickinson France SAS and the FDA: common questions

Has Becton Dickinson France SAS received an FDA warning letter?

No FDA warning letter addressed to the name "Becton Dickinson France SAS" 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 Becton Dickinson France SAS received an FDA Form 483?

FDA has not published a Form 483 for "Becton Dickinson France SAS" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Becton Dickinson France SAS?

The most recent FDA inspection on file ended Jan 25, 2013 at Le Pont-De-Claix, France and was classified VAI. FDA has 2 inspections of Becton Dickinson France SAS on file.

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