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FDA Inspection
•Cenexi Laboratoires Thissen SA•December 16, 2016

Cenexi Laboratoires Thissen SA – FDA Inspection, Dec 16, 2016

Record Details

This FDA Inspection record concerns Cenexi Laboratoires Thissen SA, with an inspection on December 16, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Cenexi Laboratoires Thissen SA
Inspection Date
December 16, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Christopher R. Czajka (FDA Associated Person)
  • Dennis Cantellops Paite (Issuing Officer)
View Company Profile

ID · 255ca1f8-d888-4de3-9151-2768b1b375e6

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1002425
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Cenexi Laboratoires Thissen SA

7
DateClassificationOfficeProject area
June 1, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 6, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 19, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 18, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 4, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Cenexi Laboratoires Thissen SA
  • FDA Inspection 1250906 - 2023-06-01
  • FDA Inspection 1192164 - 2022-12-06
  • FDA Inspection 1141824 - 2020-02-19
  • FDA Inspection 934545 - 2015-06-18
  • FDA Inspection 878521 - 2014-04-04

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