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FDA Inspection
•Octapharma Plasma, Inc.•August 10, 2015

Octapharma Plasma, Inc. – FDA Inspection, Aug 10, 2015

Record Details

This FDA Inspection record concerns Octapharma Plasma, Inc., with an inspection on August 10, 2015, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Octapharma Plasma, Inc.
Inspection Date
August 10, 2015
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 52d76d85-6aa1-4db6-8818-5bcdddc91758

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
947463
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 21 CFR 606.100(a)SOP compliance

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Octapharma Plasma, Inc.

4
DateClassificationOfficeProject area
March 1, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 24, 2018VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 21, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 20, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Octapharma Plasma, Inc.
  • FDA Inspection 1230736 - 2024-03-01
  • FDA Inspection 1053924 - 2018-05-24
  • FDA Inspection 824137 - 2013-03-21
  • FDA Inspection 824403 - 2013-03-20

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