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FDA Inspection
•Assia Chemical Industries Ltd - Teva Tech Site•September 12, 2019

Assia Chemical Industries Ltd - Teva Tech Site – FDA Inspection, Sep 12, 2019

Record Details

This FDA Inspection record concerns Assia Chemical Industries Ltd - Teva Tech Site, with an inspection on September 12, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Assia Chemical Industries Ltd - Teva Tech Site
Inspection Date
September 12, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • jose a lopez rubet (Investigator)
  • Libia M. Lugo (Issuing Officer)
View Company Profile

ID · 6f179b3e-19ac-463e-aebb-0d2a1311a1a5

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1101955
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Assia Chemical Industries Ltd - Teva Tech Site

2
DateClassificationOfficeProject area
June 6, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 30, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Assia Chemical Industries Ltd - Teva Tech Site
  • FDA Inspection 886882 - 2014-06-06
  • FDA Inspection 734906 - 2011-06-30

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