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FDA Inspection
•Thymoorgan Pharmazie Gmbh•May 22, 2014

Thymoorgan Pharmazie Gmbh – FDA Inspection, May 22, 2014

Record Details

This FDA Inspection record concerns Thymoorgan Pharmazie Gmbh, with an inspection on May 22, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Thymoorgan Pharmazie Gmbh
Inspection Date
May 22, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 399feebf-70c0-488e-be2c-a34465a28393

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
883211
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Thymoorgan Pharmazie Gmbh

7
DateClassificationOfficeProject area
April 25, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 6, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 20, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 23, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 16, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Thymoorgan Pharmazie Gmbh
  • FDA Inspection 1203954 - 2023-04-25
  • FDA Inspection 1207607 - 2022-10-06
  • FDA Inspection 1123031 - 2019-06-20
  • FDA Inspection 1053793 - 2018-04-23
  • FDA Inspection 1003153 - 2016-12-16

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