FDA Inspection 915528 — Mapa Gmbh

Mapa Gmbh — FEI 3002807642

The FDA completed an inspection of Mapa Gmbh on Feb 5, 2015 in Zeven. 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, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Zeven (Germany)

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