FDA Inspection 922785 — Mechatronic Ag

Mechatronic Ag — FEI 3008707277

The FDA completed an inspection of Mechatronic Ag on Apr 23, 2015 in Darmstadt. 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 23, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Darmstadt (Germany)

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