FDA Inspection 927252 — Nidacon International

Nidacon International — FEI 3004848623

The FDA completed an inspection of Nidacon International on May 28, 2015 in Molndal. 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
May 28, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Molndal (Sweden)

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