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 Oct 29, 2015 in Verna. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 29, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Verna (India)

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