FDA Warning Letter — SKNV

Case 507593 — FEI 3012384835

The FDA took a Warning Letter action against SKNV on Dec 21, 2016 (Pompano Beach, FL). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
SKNV
Date
Dec 21, 2016
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Pompano Beach, FL (United States)

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