American Enterprises LLC dba Sterling Gelatin

FDA Regulatory Profile

American Enterprises LLC dba Sterling Gelatin appears in FDA public data with 1 recall, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (D-062-2013, Class II) was initiated on September 21, 2012.

Summary

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

Recent Recalls

NumberClassProductDate
D-062-2013Class IILimed Bone Gelatin, packaged in six 125 kg fiber drums and labeled in part PO NO.: P8095 GELATIN 75 September 21, 2012