FDA Inspection 970676 - Teka Portugal S.A. - May 06, 2016

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Record Details

This FDA Inspection record concerns Teka Portugal S.A., with an inspection on May 6, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Teka Portugal S.A.
Inspection Date: May 6, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 2442a5c5-03c4-4d20-8271-8e349181fbe9

Violation Codes2

21 CFR 1030.10(c)(3)(i)21 CFR 1030.10(c)(3)(iii)

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