FDA Inspection 1176576 — Simmler, Inc.

Simmler, Inc. — FEI 1950226

The FDA completed an inspection of Simmler, Inc. on July 20, 2022 in Saint Louis, MO. 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 20, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)