FDA Warning Letter — Sunstone, Inc.

Case 513214 — FEI 3013096112

The FDA took a Warning Letter action against Sunstone, Inc. on Apr 17, 2017 (Pleasant Grove, UT). The action was issued by CDER and concerns drugs products.

Action Details

Facility
Sunstone, Inc.
Date
Apr 17, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Pleasant Grove, UT (United States)

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