FDA Inspection 1094271 — Robert D. Aiken, MD

Robert D. Aiken, MD — FEI 3015189649

The FDA completed an inspection of Robert D. Aiken, MD on June 26, 2019 in New Brunswick, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 26, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
New Brunswick, NJ (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
756021 CFR 312.60FD-1572, protocol compliance