FDA Inspection 1043777 — Abigo Medical AB

Abigo Medical AB — FEI 3009750086

The FDA completed an inspection of Abigo Medical AB on Feb 2, 2018 in Askersund. 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 2, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Askersund (Sweden)

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