FDA Inspection 948035 — Indoco Remedies Limited (Plant I)

Indoco Remedies Limited (Plant I) — FEI 3006644152

The FDA completed an inspection of Indoco Remedies Limited (Plant I) on October 29, 2015 in Verna. 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
October 29, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Verna (India)