FDA Inspection 933492 — Dead Sea Periclase
The FDA completed an inspection of Dead Sea Periclase on June 25, 2015 in Rotem Plants. 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
- June 25, 2015
- Fiscal Year
- 2015
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Rotem Plants (Israel)