FDA Inspection 685840 - ELOS MEDTECH PINOL A/S - September 24, 2010

Record Details

This FDA Inspection record concerns ELOS MEDTECH PINOL A/S, with an inspection on September 24, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: ELOS MEDTECH PINOL A/S
Inspection Date: September 24, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · eecbdd59-c372-42f9-ac7d-3dfa8723249f

Violation Codes2

21 CFR 820.100(a)21 CFR 820.70(e)

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