FDA Inspection 1208376 — Dennis Hammond

Dennis Hammond — FEI 3006155342

The FDA completed an inspection of Dennis Hammond on June 20, 2023 in Grand Rapids, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 20, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Grand Rapids, MI (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
300721 CFR 812.140(d)Record retention inadequate