FDA Warning Letter — MPP PHARMA LLC

Case 48779 — FEI 1930436

The FDA took a Warning Letter action against MPP PHARMA LLC on Apr 27, 2009 (Kansas City, MO). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
MPP PHARMA LLC
Date
Apr 27, 2009
Fiscal Year
2009
Product Type
Drugs
Center
CDER
Location
Kansas City, MO (United States)

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