FDA Inspection 939622 — E-Z-EM Canada, Inc

E-Z-EM Canada, Inc — FEI 3002808342

The FDA completed an inspection of E-Z-EM Canada, Inc on Aug 7, 2015 in Anjou. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Aug 7, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Anjou (Canada)

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