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FDA Inspection
•HCSC-Blood Center•July 20, 2026

HCSC-Blood Center – FDA Inspection, Jul 20, 2026

Record Details

This FDA Inspection record concerns HCSC-Blood Center, with an inspection on July 20, 2026, issued by the Philadelphia District Office, covering biologics.

Company
HCSC-Blood Center
Inspection Date
July 20, 2026
Product Type
Biologics
Office
Philadelphia District Office
People
  • Kish Bolden (Issuing Officer)
  • Michele Gottshall
View Company Profile

ID · d954c963-c909-4369-907b-a210664413ca

Inspection Facts

Inspection number
1327046
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs
  2. 21 CFR 606.160(b)Required records

Full citation text and observation details available on the Dashboard.

Other FDA inspections of HCSC-Blood Center

7
DateClassificationOfficeProject area
June 16, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 21, 2020NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 15, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 1, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 12, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 7 other inspections on the company page
Other documents for HCSC-Blood Center
  • FDA Inspection 1209789 - 2023-06-16
  • FDA Inspection 1121127 - 2020-02-21
  • FDA Inspection 1046306 - 2018-03-15
  • FDA Inspection 963579 - 2016-03-01
  • FDA Inspection 865598 - 2014-02-12

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