FDA Inspection 1271394 — NOLATO MEDITOR AB

NOLATO MEDITOR AB — FEI 3005979524

The FDA completed an inspection of NOLATO MEDITOR AB on Apr 24, 2025 in Torekov. 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
Apr 24, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Torekov (Sweden)

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