FDA Inspection 999246 — Hutchwood Enterprises, LLC DBA HCG Body Shaper
The FDA completed an inspection of Hutchwood Enterprises, LLC DBA HCG Body Shaper on January 26, 2017 in Saint Peters, 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
- January 26, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Saint Peters, MO (United States)