FDA Inspection 960749 — Fareva Morton Grove, Inc.
The FDA completed an inspection of Fareva Morton Grove, Inc. on Feb 2, 2016 in Morton Grove, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 2, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Unapproved and Misbranded Drugs
- Location
- Morton Grove, IL (United States)