FDA Inspection 1103400 — DEHAS MEDIZINTECHNIK PROJEKTIERUNG GMBH

DEHAS MEDIZINTECHNIK PROJEKTIERUNG GMBH — FEI 3013156250

The FDA completed an inspection of DEHAS MEDIZINTECHNIK PROJEKTIERUNG GMBH on Jun 19, 2019 in Lubeck. 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
Jun 19, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Lubeck (Germany)

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