FDA Inspection 1110472 — Rotem Industries Limited

Rotem Industries Limited — FEI 3008739573

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.