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FDA Inspection 748664 — Jardon Eye Prosthetics, Inc.

Jardon Eye Prosthetics, Inc. — FEI 1824736

The FDA completed an inspection of Jardon Eye Prosthetics, Inc. on October 7, 2011 in Southfield, MI. 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
October 7, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Southfield, MI (United States)

Facility

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