Arthur Schuman Midwest LLC

FDA Regulatory Profile

Arthur Schuman Midwest LLC appears in FDA public data with 1 recall — including 1 Class I (most serious) —, 0 510(k) clearances, 5 FDA inspections, and 0 compliance actions on record. Its most recent recall (F-1465-2013, Class I) was initiated on May 15, 2013.

Summary

Total Recalls
1 (1 Class I)
510(k) Clearances
0
Inspections
5
Compliance Actions
0

Recent Recalls

NumberClassProductDate
F-1465-2013Class IGRATED 2/25 GRANA PADANO; Lot Code: 313701A01; Pack Size: 2/25#; Net Pounds: 50; PACK DATE: 05/18/13May 15, 2013