FDA Inspection 1097869 — Spyder Medical
The FDA completed an inspection of Spyder Medical on May 30, 2019 in Rancho Santa Margarita, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- May 30, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Rancho Santa Margarita, CA (United States)