FDA Inspection
Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.Octapharma Pharmazeutika Produktionsgesellschaft m.b.H. – FDA Inspection, Apr 16, 2019
Record Details
This FDA Inspection record concerns Octapharma Pharmazeutika Produktionsgesellschaft m.b.H., with an inspection on April 16, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- April 16, 2019
- Product Type
- Biologics
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ID · 7c81d0cc-ae0e-4e4a-8b55-0b944d85eeff
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1090370
- FDA center
- Biologics
- Project area
- Blood and Blood Products
- Outcome
- Form 483 issued
Other FDA inspections of Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| December 16, 2022 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| January 17, 2017 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| March 5, 2015 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 18, 2012 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.
- FDA Inspection 1194258 - 2022-12-16
- FDA Inspection 1002598 - 2017-01-17
- FDA Inspection 918160 - 2015-03-05
- FDA Inspection 816229 - 2012-12-18
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