FDA Inspection 825555 — Allpack Group AG

Allpack Group AG — FEI 3004362706

The FDA completed an inspection of Allpack Group AG on Feb 22, 2013 in Reinach BL. 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 22, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Reinach BL (Switzerland)

Additional details

Postmarket Audit Inspections

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