FDA Warning Letter — Christopher D. Saudek, MD

Case 39158 — FEI 3006770163

The FDA took a Warning Letter action against Christopher D. Saudek, MD on Nov 13, 2008 (Baltimore, MD). The action was issued by CDRH and concerns devices products.

Action Details

Facility
Christopher D. Saudek, MD
Date
Nov 13, 2008
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Baltimore, MD (United States)