FDA Inspection 670601 — Eaton Manufacturing Corporation Dba Eaton Medical
The FDA completed an inspection of Eaton Manufacturing Corporation Dba Eaton Medical on June 25, 2010 in Memphis, TN. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- June 25, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Memphis, TN (United States)