FDA Inspection 1302492 — PAMA Manufacturing & Sterilization

PAMA Manufacturing & Sterilization — FEI 3010547268

The FDA completed an inspection of PAMA Manufacturing & Sterilization on Dec 10, 2025 in Mirabel. 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
Dec 10, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mirabel (Canada)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.