FDA Inspection 921358 — 2035 PMA
The FDA completed an inspection of 2035 PMA on Apr 3, 2015 in Rapid City, SD. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI)
- End Date
- Apr 3, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Rapid City, SD (United States)