FDA Inspection 1155847 — Teva API India Ltd- Malanpur

Teva API India Ltd- Malanpur — FEI 3008256596

The FDA completed an inspection of Teva API India Ltd- Malanpur on November 28, 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
November 28, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bhind (India)

Additional Details

Mutual Recognition Agreement (MRA)