FDA Inspection 1086616 — Teva API India Ltd- Malanpur

Teva API India Ltd- Malanpur — FEI 3008256596

The FDA completed an inspection of Teva API India Ltd- Malanpur on April 16, 2019 in Bhind. 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
April 16, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bhind (India)