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FDA Inspection
•BioLife Plasma Services, L.P.•June 13, 2011

BioLife Plasma Services, L.P. – FDA Inspection, Jun 13, 2011

Record Details

This FDA Inspection record concerns BioLife Plasma Services, L.P., with an inspection on June 13, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
BioLife Plasma Services, L.P.
Inspection Date
June 13, 2011
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 20545f37-0728-4549-8059-2c0c51d42ac4

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
729579
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 21 CFR 606.171Biological product deviation report

Full citation text and observation details available on the Dashboard.

Other FDA inspections of BioLife Plasma Services, L.P.

7
DateClassificationOfficeProject area
July 12, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 24, 2017NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 1, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 22, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 28, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 7 other inspections on the company page
Other documents for BioLife Plasma Services, L.P.
  • FDA Inspection 1211552 - 2023-07-12
  • FDA Inspection 1014522 - 2017-05-24
  • FDA Inspection 993744 - 2016-12-01
  • FDA Inspection 934450 - 2015-06-22
  • FDA Inspection 846130 - 2013-08-28

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