FDA Inspection 1008978 — Adhexpharma

Adhexpharma — FEI 3008426496

The FDA completed an inspection of Adhexpharma on Feb 3, 2017 in Chenove. 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 3, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Chenove (France)

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