GlaxoSmithKline Biologicals SA FDA Record

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

GlaxoSmithKline Biologicals SA has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "GlaxoSmithKline Biologicals SA" is on file. FDA has published 3 Form 483s for GlaxoSmithKline Biologicals SA.

What these totals cover: FDA records filed under the name "GlaxoSmithKline Biologicals SA" and its spelling variant "Glaxosmithkline Biologicals". They do not include records filed under Glaxosmithkline or other names in its corporate family; those are listed under Related names, each with its own counts.

Latest recall
D-0544-2024 · May 17, 2024 · filed under Glaxosmithkline
Latest inspection
Mar 12, 2024 · VAI

Newer recall under related name Glaxosmithkline: May 17, 2024, D-0544-2024.

Part of the Glaxosmithkline corporate family.

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

FDA record by year

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

GlaxoSmithKline Biologicals SA: FDA inspections per year 2017: 1 inspections120172018: 0 inspections020182019: 0 inspections020192020: 0 inspections020202021: 0 inspections020212022: 2 inspections220222023: 1 inspections120232024: 1 inspections120242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202410000
202310000
202220000
202100000
202000000
201900000
201800000
201710000

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.

GlaxoSmithKline Biologicals SA Form 483s

3 Form 483s published by FDA.

DateDocumentFEI
Feb 27, 20264833003973577
Mar 12, 20244833014752610
Jun 24, 20194833002875226

A Form 483 lists the observations FDA investigators made at the end of an inspection. FDA publishes some Form 483s in its reading room, and each date links to that document. Read the observations with the FDA 483 search.

Recent FDA inspections

8 inspections from Jun 3, 2010 to Mar 12, 2024.

DateSiteProductClassificationFEI
Mar 12, 2024Saint-Amand-Les-Eaux, FranceBiologicsVoluntary Action Indicated (VAI)3014752610
Jun 23, 2023Rixensart, BelgiumBiologicsNo Action Indicated (NAI)3002875226
Nov 8, 2022Singapore, SingaporeBiologicsVoluntary Action Indicated (VAI)3016007176
Sep 13, 2022Saint-Amand-Les-Eaux, FranceBiologicsVoluntary Action Indicated (VAI)3014752610
Jan 27, 2017Rixensart, BelgiumBiologicsVoluntary Action Indicated (VAI)3002875226
Oct 2, 2014Rixensart, BelgiumBiologicsVoluntary Action Indicated (VAI)3002875226
Oct 5, 2012Rixensart, BelgiumBiologicsVoluntary Action Indicated (VAI)3002875226
Jun 3, 2010Rixensart, BelgiumBiologicsVoluntary Action Indicated (VAI)3002875226
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

3 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3014752610Saint-Amand-Les-Eaux, France2Mar 12, 2024
FEI 3002875226Rixensart, Belgium5Jun 23, 2023
FEI 3016007176Singapore, Singapore1Nov 8, 2022

GlaxoSmithKline Biologicals SA and the FDA: common questions

Has GlaxoSmithKline Biologicals SA received an FDA warning letter?

No FDA warning letter addressed to the name "GlaxoSmithKline Biologicals SA" 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 GlaxoSmithKline Biologicals SA received an FDA Form 483?

FDA has published 3 Form 483s for GlaxoSmithKline Biologicals SA in its reading room, the most recent dated Feb 27, 2026. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect GlaxoSmithKline Biologicals SA?

The most recent FDA inspection on file ended Mar 12, 2024 at Saint-Amand-Les-Eaux, France and was classified VAI. FDA has 8 inspections of GlaxoSmithKline Biologicals SA on file.

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