FDA Inspection 1086611 — SigmaGraft Inc

SigmaGraft Inc — FEI 3009598981

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.