Penner Mfg Inc

FDA Regulatory Profile

Penner Mfg Inc appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1306-2015, Class II) was initiated on January 30, 2015.

Summary

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

Recent Recalls

NumberClassProductDate
Z-1306-2015Class IIPenner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific Stretcher/January 30, 2015