FDA Inspection 1214924 — Synthasome, Inc

Synthasome, Inc — FEI 3008008164

The FDA completed an inspection of Synthasome, Inc on July 18, 2023 in Del Mar, 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 18, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Del Mar, CA (United States)