FDA Warning Letter — Diasol, Inc

Case 121048 — FEI 3007137482

The FDA took a Warning Letter action against Diasol, Inc on Aug 9, 2010 (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
Aug 9, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Phoenix, AZ (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.