FDA Inspection 1224759 — Memry Corporation

Memry Corporation — FEI 3004579081

The FDA completed an inspection of Memry Corporation on December 1, 2023 in Bethel, CT. 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
December 1, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Bethel, CT (United States)