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FDA Inspection 974523 — Novo Nordisk Pharmatech A/S

Novo Nordisk Pharmatech A/S — FEI 3008618737

The FDA completed an inspection of Novo Nordisk Pharmatech A/S on Jun 3, 2016 in Koge. 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
Jun 3, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Koge (Denmark)

Facility

Other inspections at this facility

FDA data resources

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