FDA Inspection
GlaxoSmithKline LLCGlaxoSmithKline LLC – FDA Inspection, Apr 21, 2016
Record Details
This FDA Inspection record concerns GlaxoSmithKline LLC, with an inspection on April 21, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- GlaxoSmithKline LLC
- Inspection Date
- April 21, 2016
- Product Type
- Drugs
View Company Profile
ID · cc81defe-1000-49a7-8e5a-3c8096621bd1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 987392
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.198(a)Complaint Handling Procedure
- 21 CFR 211.192Investigations of discrepancies, failures
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Other FDA inspections of GlaxoSmithKline LLC
8| Date | Classification | Office | Project area |
|---|---|---|---|
| February 20, 2026 | Not classified | Atlanta District Office | |
| April 19, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 26, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 21, 2015 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 3, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for GlaxoSmithKline LLC
- FDA Inspection 1298596 - 2026-02-20
- FDA Inspection 1229588 - 2024-04-19
- FDA Inspection 1043270 - 2018-01-26
- FDA Inspection 940149 - 2015-08-21
- FDA Inspection 841675 - 2013-05-03
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