FDA Warning Letter — Diasol, Inc

Case 719460 — FEI 3007137482

The FDA took a Warning Letter action against Diasol, Inc on January 30, 2026 (Phoenix, AZ). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Diasol, Inc
Date
January 30, 2026
Fiscal Year
2026
Product Type
Devices
Center
CDRH
Location
Phoenix, AZ (United States)