FDA Inspection 884520 — Satyaprakash N. Makam, MD

Satyaprakash N. Makam, MD — FEI 3009018121

The FDA completed an inspection of Satyaprakash N. Makam, MD on May 23, 2014 in Munster, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 23, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Munster, IN (United States)

Additional Details

Clinical Investigator (CI)