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FDA Inspection 753658 — Teco Diagnostics, Inc.

Teco Diagnostics, Inc. — FEI 1832216

The FDA completed an inspection of Teco Diagnostics, Inc. on October 14, 2011 in Anaheim, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
October 14, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Anaheim, CA (United States)

Facility

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Recent compliance actions

FDA data resources