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FDA Inspection
•OneBlood, Inc.•May 11, 2009

OneBlood, Inc. – FDA Inspection, May 11, 2009

Record Details

This FDA Inspection record concerns OneBlood, Inc., with an inspection on May 11, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
OneBlood, Inc.
Inspection Date
May 11, 2009
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 02971630-cd16-41c3-a6d9-0c4bee22430e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
582281
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 21 CFR 211.100(b)SOPs not followed / documented

Full citation text and observation details available on the Dashboard.

Other FDA inspections of OneBlood, Inc.

6
DateClassificationOfficeProject area
February 25, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
January 17, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 10, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 2, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 12, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for OneBlood, Inc.
  • FDA Inspection 1163513 - 2022-02-25
  • FDA Inspection 1077142 - 2019-01-17
  • FDA Inspection 997028 - 2016-11-10
  • FDA Inspection 906018 - 2014-12-02
  • FDA Inspection 818857 - 2013-02-12

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