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FDA Inspection
•American Red Cross-Myrtle Beach•October 29, 2010

American Red Cross-Myrtle Beach – FDA Inspection, Oct 29, 2010

Record Details

This FDA Inspection record concerns American Red Cross-Myrtle Beach, with an inspection on October 29, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
American Red Cross-Myrtle Beach
Inspection Date
October 29, 2010
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · e4380860-fe7a-461d-8131-a8572a56af2c

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
696847
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs

Full citation text and observation details available on the Dashboard.

Other FDA inspections of American Red Cross-Myrtle Beach

5
DateClassificationOfficeProject area
July 9, 2026Not classifiedAtlanta District Office
April 6, 2023NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
August 2, 2017NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 24, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 29, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for American Red Cross-Myrtle Beach
  • FDA Inspection 1330826 - 2026-07-09
  • FDA Inspection 1204031 - 2023-04-06
  • FDA Inspection 1021137 - 2017-08-02
  • FDA Inspection 931618 - 2015-06-24
  • FDA Inspection 846755 - 2013-08-29

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