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FDA Inspection
•OneBlood, Inc.•April 8, 2019

FDA Inspection 1085562 - OneBlood, Inc. - April 08, 2019

Record Details

This FDA Inspection record concerns OneBlood, Inc., with an inspection on April 8, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
OneBlood, Inc.
Inspection Date
April 8, 2019
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 651a651b-67c5-4b38-86c8-9764e9e7a058

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1085562
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 21 CFR 606.100(c)Thorough investigations

Full citation text and observation details available on the Dashboard.

Other FDA inspections of OneBlood, Inc.

5
DateClassificationOfficeProject area
March 12, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 23, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 6, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 1, 2012NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 13, 2010NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for OneBlood, Inc.
  • FDA Inspection 1234208 - 2024-03-12
  • FDA Inspection 971831 - 2016-03-23
  • FDA Inspection 890524 - 2014-08-06
  • FDA Inspection 771878 - 2012-03-01
  • FDA Inspection 661908 - 2010-05-13

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