FDA Inspection 752838 - Henthorn Ocular Prosthetics - November 09, 2011

FDA Inspection 752838 for Henthorn Ocular Prosthetics on November 09, 2011. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 752838 for Henthorn Ocular Prosthetics on November 09, 2011. Classification: No Action Indicated (NAI).

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Record Information

Company

Henthorn Ocular Prosthetics

Inspection Date

November 9, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f6884471-8733-4adb-9d6d-9466c0086cba

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