FDA Inspection 1110472 — Rotem Industries Limited

Rotem Industries Limited — FEI 3008739573

The FDA completed an inspection of Rotem Industries Limited on November 7, 2019 in Dimona. 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 7, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dimona (Israel)