FDA Inspection
Octapharma Plasma, Inc. PortsmouthOctapharma Plasma, Inc. Portsmouth – FDA Inspection, Jun 28, 2011
Record Details
This FDA Inspection record concerns Octapharma Plasma, Inc. Portsmouth, with an inspection on June 28, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- June 28, 2011
- Product Type
- Biologics
View Company Profile
ID · ffecfff3-542f-4658-858f-176088ee823f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 733852
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
1- 21 CFR 1271.270(a)Accurate, indelible, legible
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Other FDA inspections of Octapharma Plasma, Inc. Portsmouth
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 30, 2021 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| September 26, 2018 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| October 28, 2016 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| June 20, 2013 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Octapharma Plasma, Inc. Portsmouth
- FDA Inspection 1137609 - 2021-03-30
- FDA Inspection 1066750 - 2018-09-26
- FDA Inspection 992370 - 2016-10-28
- FDA Inspection 838033 - 2013-06-20
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