FDA Inspection 718609 — Eaton Manufacturing Corporation Dba Eaton Medical
The FDA completed an inspection of Eaton Manufacturing Corporation Dba Eaton Medical on March 28, 2011 in Memphis, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- March 28, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Memphis, TN (United States)