FDA Inspection 816590 — Fertipro N.V.

Fertipro N.V. — FEI 3003272500

The FDA completed an inspection of Fertipro N.V. on Dec 6, 2012 in Beernem. 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
Dec 6, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Beernem (Belgium)

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