FDA Inspection 665333 — 2035 PMA
The FDA completed an inspection of 2035 PMA on May 27, 2010 in Rapid City, SD. 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
- May 27, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Rapid City, SD (United States)