FDA Inspection 975283 — Genus Medical Technologies
The FDA completed an inspection of Genus Medical Technologies on June 8, 2016 in Chesterfield, MO. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- June 8, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Unapproved and Misbranded Drugs
- Location
- Chesterfield, MO (United States)