FDA Warning Letter — Andapharm, LLC

Case 438600 — FEI 3005000348

The FDA took a Warning Letter action against Andapharm, LLC on Aug 26, 2014 (Fort Lauderdale, FL). The action was issued by CDER and concerns drugs products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Andapharm, LLC
Date
Aug 26, 2014
Fiscal Year
2014
Product Type
Drugs
Center
CDER
Location
Fort Lauderdale, FL (United States)

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