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FDA Inspection
•Memorial Hermann Texas Medical Center•November 16, 2017

Memorial Hermann Texas Medical Center – FDA Inspection, Nov 16, 2017

Record Details

This FDA Inspection record concerns Memorial Hermann Texas Medical Center, with an inspection on November 16, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Memorial Hermann Texas Medical Center
Inspection Date
November 16, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Darla J. Christopher (FDA Associated Person)
View Company Profile

ID · fcf1eced-1939-4c2d-ba95-5b429234b2a3

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1031447
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 606.171Biological product deviation report

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Memorial Hermann Texas Medical Center

6
DateClassificationOfficeProject area
November 18, 2024Not classifiedDallas District Office
August 26, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
June 10, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 14, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 26, 2012NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Memorial Hermann Texas Medical Center
  • FDA Inspection 1256951 - 2024-11-18
  • FDA Inspection 1180562 - 2022-08-26
  • FDA Inspection 985572 - 2016-06-10
  • FDA Inspection 862714 - 2014-01-14
  • FDA Inspection 773663 - 2012-03-26

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