FDA Warning Letter — Topspins, Inc.

Case 438886 — FEI 3000717685

The FDA took a Warning Letter action against Topspins, Inc. on November 6, 2014 (Ann Arbor, MI). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Topspins, Inc.
Date
November 6, 2014
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Ann Arbor, MI (United States)