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FDA Inspection
•UAB Teva Baltics•May 11, 2018

UAB Teva Baltics – FDA Inspection, May 11, 2018

Record Details

This FDA Inspection record concerns UAB Teva Baltics, with an inspection on May 11, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
UAB Teva Baltics
Inspection Date
May 11, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • John P. Mistler (FDA Associated Person)
View Company Profile

ID · 177a66f6-fbfe-47b7-bb59-a885ff9dc2c2

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1057580
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of UAB Teva Baltics

3
DateClassificationOfficeProject area
May 9, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 23, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 3, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for UAB Teva Baltics
  • FDA Inspection 1270427 - 2024-05-09
  • FDA Inspection 1124668 - 2019-05-23
  • FDA Inspection 933280 - 2015-07-03

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