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FDA Inspection 831948 — Teco Diagnostics, Inc.

Teco Diagnostics, Inc. — FEI 1832216

The FDA completed an inspection of Teco Diagnostics, Inc. on April 4, 2013 in Anaheim, 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
April 4, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Anaheim, CA (United States)

Facility

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Recent compliance actions

FDA data resources