FDA Inspection 1194250 — Cenova AB

Cenova AB — FEI 3005216725

The FDA completed an inspection of Cenova AB on Nov 18, 2022 in Mjolby. 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 18, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Mjolby (Sweden)

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