Arnold Tuber Industries

FDA Regulatory Profile

Arnold Tuber Industries appears in FDA public data with 0 recalls, 1 510(k) clearance, 8 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on December 11, 2009.

Summary

Total Recalls
0
510(k) Clearances
1
Inspections
8
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K092943ASPIRATING SYRINGE, NON-ASPIRATING SYRINGEDecember 11, 2009