FDA Inspection 1230975 — Magna Pharmaceuticals Inc

Magna Pharmaceuticals Inc — FEI 3007457368

The FDA completed an inspection of Magna Pharmaceuticals Inc on Feb 5, 2024 in Louisville, KY. 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
Feb 5, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Louisville, KY (United States)

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