FDA Inspection
SmithKline Beecham Pharma GmbH & co. KG (dba GlaxoSmithKline Biologicals)SmithKline Beecham Pharma GmbH & co. KG (dba GlaxoSmithKline Biologicals) – FDA Inspection, Jun 27, 2017
Record Details
This FDA Inspection record concerns SmithKline Beecham Pharma GmbH & co. KG (dba GlaxoSmithKline Biologicals), with an inspection on June 27, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- June 27, 2017
- Product Type
- Biologics
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ID · e4847276-f3f0-4073-a7d2-e60f6d62c3c5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1019795
- FDA center
- Biologics
- Project area
- Vaccines and Allergenic Products
- Outcome
- Form 483 issued
Other FDA inspections of SmithKline Beecham Pharma GmbH & co. KG (dba GlaxoSmithKline Biologicals)
6| Date | Classification | Office | Project area |
|---|---|---|---|
| March 15, 2024 | VAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| September 20, 2022 | VAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| July 5, 2019 | NAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| June 22, 2011 | VAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| May 24, 2010 | VAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
Other documents for SmithKline Beecham Pharma GmbH & co. KG (dba GlaxoSmithKline Biologicals)
- FDA Inspection 1233707 - 2024-03-15
- FDA Inspection 1181891 - 2022-09-20
- FDA Inspection 1101506 - 2019-07-05
- FDA Inspection 736162 - 2011-06-22
- FDA Inspection 668686 - 2010-05-24
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