FDA Inspection 1032329 — Noramco, Inc.

Noramco, Inc. — FEI 2522445

The FDA completed an inspection of Noramco, Inc. on Nov 17, 2017 in Wilmington, DE. 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). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 17, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wilmington, DE (United States)

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