FDA Inspection 1054420 — Veda Lab

Veda Lab — FEI 3000254998

The FDA completed an inspection of Veda Lab on Mar 1, 2018 in Alancon. 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
Mar 1, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Alancon (France)

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