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FDA Inspection 944716 — Medart A /S

Medart A /S — FEI 3005616124

The FDA completed an inspection of Medart A /S on Sep 24, 2015 in Hvidovre. 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
Sep 24, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Hvidovre (Denmark)

Facility

Other inspections at this facility

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FDA data resources

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