FDA Inspection 1097344 — Sparqtron Corporation

Sparqtron Corporation — FEI 3002736133

The FDA completed an inspection of Sparqtron Corporation on July 11, 2019 in Fremont, 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
July 11, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Fremont, CA (United States)