FDA Inspection 1086611 — SigmaGraft Inc

SigmaGraft Inc — FEI 3009598981

The FDA completed an inspection of SigmaGraft Inc on March 7, 2019 in Fullerton, 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
March 7, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Fullerton, CA (United States)