FDA Inspection 1277698 — Simmler, Inc.

Simmler, Inc. — FEI 1950226

The FDA completed an inspection of Simmler, Inc. on August 5, 2025 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
August 5, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)