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FDA Inspection
•LifeServe Blood Center•May 28, 2014

LifeServe Blood Center – FDA Inspection, May 28, 2014

Record Details

This FDA Inspection record concerns LifeServe Blood Center, with an inspection on May 28, 2014, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
LifeServe Blood Center
Inspection Date
May 28, 2014
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 062a96e0-e3eb-4d80-be3d-575713d489b0

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
884950
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

3
  1. 21 CFR 606.40(a)(1)Provide space for examination
  2. 21 CFR 211.100(b)SOPs not followed / documented
  3. 21 CFR 606.170(a)Adverse Reaction- Reports of Investigations

Full citation text and observation details available on the Dashboard.

Other FDA inspections of LifeServe Blood Center

10
DateClassificationOfficeProject area
November 22, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 18, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 23, 2018NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
August 8, 2017NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 1, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 10 other inspections on the company page
Other documents for LifeServe Blood Center
  • FDA Inspection 1257768 - 2024-11-22
  • FDA Inspection 1105239 - 2019-09-18
  • FDA Inspection 1068080 - 2018-08-23
  • FDA Inspection 1022900 - 2017-08-08
  • FDA Inspection 979671 - 2016-07-01

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