FDA Inspection 599948 — Permobil Inc
The FDA completed an inspection of Permobil Inc on July 21, 2009 in Lebanon, TN. 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
- July 21, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lebanon, TN (United States)