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FDA Inspection
•LifeSouth Community Blood Centers Inc•November 14, 2011

LifeSouth Community Blood Centers Inc – FDA Inspection, Nov 14, 2011

Record Details

This FDA Inspection record concerns LifeSouth Community Blood Centers Inc, with an inspection on November 14, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
LifeSouth Community Blood Centers Inc
Inspection Date
November 14, 2011
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 2a59bf56-d2be-4426-a5db-5692c39a6069

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
753212
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

15
  1. 21 CFR 606.100(c)Record review prior to release
  2. 21 CFR 606.165(b)Distribution records - content
  3. 21 CFR 606.60(a)Provide proper equipment to meet requirements
  4. 21 CFR 640.11(b)General requirements - inspection
  5. 21 CFR 606.160(b)Required records
  6. 21 CFR 606.100(c)Thorough investigations
  7. 21 CFR 640.11(a)General requirements - storage
  8. 21 CFR 640.25(a)Storage temps./agitation
  9. 21 CFR 606.171Biological product deviation report
  10. 21 CFR 606.65(e)Following manufacturer"s instructions

Showing 10 of 15 citations.

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Other FDA inspections of LifeSouth Community Blood Centers Inc

7
DateClassificationOfficeProject area
September 10, 2025VAINew Orleans District OfficeBlood and Blood Products
October 28, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
March 12, 2020NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
August 18, 2017NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 10, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 7 other inspections on the company page
Other documents for LifeSouth Community Blood Centers Inc
  • FDA Inspection 1281079 - 2025-09-10
  • FDA Inspection 1190252 - 2022-10-28
  • FDA Inspection 1122834 - 2020-03-12
  • FDA Inspection 1029818 - 2017-08-18
  • FDA Inspection 933401 - 2015-07-10

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