FDA Inspection 1255752 — Passy-Muir, Inc.

Passy-Muir, Inc. — FEI 2024841

The FDA completed an inspection of Passy-Muir, Inc. on Nov 1, 2024 in Irvine, CA. 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
Nov 1, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)