FDA Inspection 1097869 — Spyder Medical

Spyder Medical — FEI 3013437289

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 were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 30, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Rancho Santa Margarita, CA (United States)