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FDA Inspection
•OneBlood, Inc.•September 24, 2010

OneBlood, Inc. – FDA Inspection, Sep 24, 2010

Record Details

This FDA Inspection record concerns OneBlood, Inc., with an inspection on September 24, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
OneBlood, Inc.
Inspection Date
September 24, 2010
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 33d6a7ec-60d0-4f35-ac78-e7f881edbc32

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
680208
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 21 CFR 606.160(a)(1)Concurrent documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of OneBlood, Inc.

8
DateClassificationOfficeProject area
March 27, 2025NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 22, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 31, 2020NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 25, 2017NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
October 20, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 8 other inspections on the company page
Other documents for OneBlood, Inc.
  • FDA Inspection 1266322 - 2025-03-27
  • FDA Inspection 1219444 - 2023-09-22
  • FDA Inspection 1121674 - 2020-01-31
  • FDA Inspection 1028525 - 2017-08-25
  • FDA Inspection 945730 - 2015-10-20

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