FDA Inspection 1229588 — GlaxoSmithKline LLC

GlaxoSmithKline LLC — FEI 1033964

The FDA completed an inspection of GlaxoSmithKline LLC on Apr 19, 2024 in Zebulon, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 19, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Zebulon, NC (United States)

Citations

IDCFRDescription
241921 CFR 211.198(a)Complaint Handling Procedure

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