FDA Inspection 886604 — Pro-Tech Design & Manufacturing, Inc.

Pro-Tech Design & Manufacturing, Inc. — FEI 3003574398

The FDA completed an inspection of Pro-Tech Design & Manufacturing, Inc. on June 12, 2014 in Santa Fe Springs, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 12, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Fe Springs, CA (United States)