FDA Warning Letter — Manish Mehta, MD

Case 254754 — FEI 3009579540

The FDA took a Warning Letter action against Manish Mehta, MD on February 21, 2012 (Albany, NY). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Manish Mehta, MD
Date
February 21, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Albany, NY (United States)