FDA Inspection 1007877 — Dexcel Ltd.

Dexcel Ltd. — FEI 3002806801

The FDA completed an inspection of Dexcel Ltd. on February 16, 2017 in Or Akiva. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 16, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Or Akiva (Israel)