FDA Inspection 847310 — Organon Heist

Organon Heist — FEI 3003974846

The FDA completed an inspection of Organon Heist on Sep 5, 2013 in Heist-Op-Den-Berg. 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
Sep 5, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Heist-Op-Den-Berg (Belgium)

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