FDA Inspection 1002017 — Dunnick, Cory A. MD

Dunnick, Cory A. MD — FEI 3013170810

The FDA completed an inspection of Dunnick, Cory A. MD on Feb 27, 2017 in Aurora, CO. 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). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 27, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Aurora, CO (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
748821 CFR 312.59Records of unused drug disposition
756021 CFR 312.60FD-1572, protocol compliance

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