FDA Inspection 671362 — Hawkeye Jensen Inc

Hawkeye Jensen Inc — FEI 3001600976

The FDA completed an inspection of Hawkeye Jensen Inc on July 14, 2010 in Shartlesville, PA. 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
July 14, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Shartlesville, PA (United States)