FDA Warning Letter — Raritan Pharmaceuticals, Inc.

Case 516099 — FEI 3004083931

The FDA took a Warning Letter action against Raritan Pharmaceuticals, Inc. on Jun 20, 2017 (East Brunswick, NJ). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Raritan Pharmaceuticals, Inc.
Date
Jun 20, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
East Brunswick, NJ (United States)

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