FDA Warning Letter — Schindele Enterprises dba Midwest Wholesale

Case 418843 — FEI 3010346131

The FDA took a Warning Letter action against Schindele Enterprises dba Midwest Wholesale on July 17, 2014 (Nixa, MO). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Schindele Enterprises dba Midwest Wholesale
Date
July 17, 2014
Fiscal Year
2014
Product Type
Drugs
Center
CDER
Location
Nixa, MO (United States)