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FDA Inspection
•Trident Medical Center•August 17, 2010

Trident Medical Center – FDA Inspection, Aug 17, 2010

Record Details

This FDA Inspection record concerns Trident Medical Center, with an inspection on August 17, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Trident Medical Center
Inspection Date
August 17, 2010
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · fad893f7-698b-4fd3-ab98-9ffbc41c8c30

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
676544
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

2
  1. 21 CFR 606.60(a)Equipment observed, standardized, calibrated
  2. 21 CFR 606.160(b)Required records

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Trident Medical Center

4
DateClassificationOfficeProject area
June 13, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 9, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 30, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 24, 2012NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Trident Medical Center
  • FDA Inspection 1056706 - 2018-06-13
  • FDA Inspection 973245 - 2016-06-09
  • FDA Inspection 878148 - 2014-04-30
  • FDA Inspection 797329 - 2012-08-24

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