FDA Inspection 1262424 — M.R.S. SRL

M.R.S. SRL — FEI 3010608097

The FDA completed an inspection of M.R.S. SRL on Jan 16, 2025 in Gazzaniga. 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
Jan 16, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Gazzaniga (Italy)

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