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FDA Inspection
•BioLife Plasma Services, L.P.•July 31, 2009

BioLife Plasma Services, L.P. – FDA Inspection, Jul 31, 2009

Record Details

This FDA Inspection record concerns BioLife Plasma Services, L.P., with an inspection on July 31, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
BioLife Plasma Services, L.P.
Inspection Date
July 31, 2009
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · a744b206-9bc2-430e-bd17-2d0e25144652

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
611304
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

2
  1. 21 CFR 606.160(a)(2)Determination of lot numbers and supplies
  2. 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs

Full citation text and observation details available on the Dashboard.

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

6
DateClassificationOfficeProject area
April 24, 2026NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 26, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 3, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 11, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 2, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for BioLife Plasma Services, L.P.
  • FDA Inspection 1315498 - 2026-04-24
  • FDA Inspection 1211622 - 2023-07-26
  • FDA Inspection 992474 - 2016-11-03
  • FDA Inspection 917180 - 2015-03-11
  • FDA Inspection 816633 - 2013-02-02

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