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FDA Inspection
•Oklahoma Blood Institute Arkansas Blood Institute•July 20, 2018

Oklahoma Blood Institute Arkansas Blood Institute – FDA Inspection, Jul 20, 2018

Record Details

This FDA Inspection record concerns Oklahoma Blood Institute Arkansas Blood Institute, with an inspection on July 20, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Oklahoma Blood Institute Arkansas Blood Institute
Inspection Date
July 20, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Eric T. Huebler (Issuing Officer)
View Company Profile

ID · 620e8ad3-5e3b-45bb-af67-02c304a47923

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1060711
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

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 Oklahoma Blood Institute Arkansas Blood Institute

4
DateClassificationOfficeProject area
February 6, 2025NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 28, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
October 19, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
October 6, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Oklahoma Blood Institute Arkansas Blood Institute
  • FDA Inspection 1261481 - 2025-02-06
  • FDA Inspection 1169916 - 2022-04-28
  • FDA Inspection 989311 - 2016-10-19
  • FDA Inspection 946357 - 2015-10-06

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