FDA Inspection 830061 — Novo Nordisk A/S

Novo Nordisk A/S — FEI 3004547341

The FDA completed an inspection of Novo Nordisk A/S on Mar 21, 2013 in Hjorring. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 21, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Hjorring (Denmark)

Citations

IDCFRDescription
328621 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate

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