FDA Inspection 831157 - Steritec Products Mfg. Co., Inc. - May 01, 2013

FDA Inspection 831157 for Steritec Products Mfg. Co., Inc. on May 01, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 831157 for Steritec Products Mfg. Co., Inc. on May 01, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Steritec Products Mfg. Co., Inc.

Inspection Date

May 1, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa054a24-804c-4708-8b8e-8b1c5e809ef7

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