FDA Warning Letter — Entellus Medical Inc.

Case 511495 — FEI 3006345872

The FDA took a Warning Letter action against Entellus Medical Inc. on April 6, 2017 (Plymouth, MN). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Entellus Medical Inc.
Date
April 6, 2017
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Plymouth, MN (United States)