FDA Inspection 1028985 — Michael L. Nordlund, MD, PhD

Michael L. Nordlund, MD, PhD — FEI 3013828253

The FDA completed an inspection of Michael L. Nordlund, MD, PhD on Oct 18, 2017 in Blue Ash, OH. 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 18, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Blue Ash, OH (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
753021 CFR 312.62(b)Case history records- inadequate or inadequate

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