FDA Inspection 880903 — Composite Manufacturing, Inc

Composite Manufacturing, Inc — FEI 1000519805

The FDA completed an inspection of Composite Manufacturing, Inc on May 29, 2014 in San Clemente, 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)
End Date
May 29, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
San Clemente, CA (United States)