FDA Inspection 1092599 — Moog Aspen Motion Technologies
The FDA completed an inspection of Moog Aspen Motion Technologies on April 18, 2019 in Radford, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- April 18, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Radford, VA (United States)