FDA Inspection 1179020 — Syntermed, Inc.

Syntermed, Inc. — FEI 3003079232

The FDA completed an inspection of Syntermed, Inc. on Aug 11, 2022 in Atlanta, GA. 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
Aug 11, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Atlanta, GA (United States)