FDA Warning Letter — Sepal Reproductive Devices, Inc.

Case 115928 — FEI 3003803140

The FDA took a Warning Letter action against Sepal Reproductive Devices, Inc. on October 1, 2010 (Boston, MA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Sepal Reproductive Devices, Inc.
Date
October 1, 2010
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Boston, MA (United States)