FDA Inspection 994376 — Coltene/Whaledent Gmbh + Co. KG

Coltene/Whaledent Gmbh + Co. KG — FEI 3001180585

The FDA completed an inspection of Coltene/Whaledent Gmbh + Co. KG on Nov 16, 2016 in Langenau. 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 16, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Langenau (Germany)

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