Precision Valve & Automation,Inc

FDA Regulatory Profile

Precision Valve & Automation,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-2805-2020, Class II) was initiated on June 26, 2020.

Summary

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

Recent Recalls

NumberClassProductDate
Z-2805-2020Class IIPVA, PREVENT is an FDA-authorized emergency ventilator designed to treat patients suffering from COVJune 26, 2020