FDA Inspection 1098333 — Oxalis Labs

Oxalis Labs — FEI 3010868532

The FDA completed an inspection of Oxalis Labs on August 2, 2019 in Solan. 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
August 2, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Solan (India)