FDA Warning Letter — Surgisil, LLP

Case 567886 — FEI 3006007116

The FDA took a Warning Letter action against Surgisil, LLP on April 15, 2019 (Plano, TX). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Surgisil, LLP
Date
April 15, 2019
Fiscal Year
2019
Product Type
Devices
Center
CDRH
Location
Plano, TX (United States)