FDA Inspection 580472 — Lightmed USA Inc
The FDA completed an inspection of Lightmed USA Inc on January 28, 2009 in San Clemente, CA. 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
- January 28, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- San Clemente, CA (United States)