FDA Warning Letter — Skytron, LLC

Case 723950 — FEI 1825014

The FDA took a Warning Letter action against Skytron, LLC on May 19, 2026 (Grand Rapids, MI). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Skytron, LLC
Date
May 19, 2026
Fiscal Year
2026
Product Type
Devices
Center
CDRH
Location
Grand Rapids, MI (United States)