FDA Warning Letter — Satyaprakash N. Makam, MD

Case 235534 — FEI 3009018121

The FDA took a Warning Letter action against Satyaprakash N. Makam, MD on December 19, 2011 (Munster, IN). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Satyaprakash N. Makam, MD
Date
December 19, 2011
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Munster, IN (United States)