FDA Inspection 838129 - Zest Anchors LLC - June 27, 2013

FDA Inspection 838129 for Zest Anchors LLC on June 27, 2013. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 838129 for Zest Anchors LLC on June 27, 2013. Classification: No Action Indicated (NAI).

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Record Information

Company

Zest Anchors LLC

Inspection Date

June 27, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa13ffd8-2d39-41c8-a2b5-fca3a6564e42

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