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FDA Inspection
•Terrebonne General Health System•February 25, 2010

Terrebonne General Health System – FDA Inspection, Feb 25, 2010

Record Details

This FDA Inspection record concerns Terrebonne General Health System, with an inspection on February 25, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Terrebonne General Health System
Inspection Date
February 25, 2010
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 76136435-72a7-4f65-bf8b-1beee580a5ca

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
657774
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

2
  1. 21 CFR 606.100(c)Record review prior to release
  2. 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 Terrebonne General Health System

7
DateClassificationOfficeProject area
September 9, 2025Not classifiedNew Orleans District Office
August 24, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 28, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 10, 2017VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 2, 2015VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 7 other inspections on the company page
Other documents for Terrebonne General Health System
  • FDA Inspection 1283764 - 2025-09-09
  • FDA Inspection 1217492 - 2023-08-24
  • FDA Inspection 1102308 - 2019-08-28
  • FDA Inspection 1000028 - 2017-02-10
  • FDA Inspection 928625 - 2015-06-02

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