FDA Inspection 1100229 - Precision Systems, Inc. - August 14, 2019

FDA Inspection 1100229 for Precision Systems, Inc. on August 14, 2019. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1100229 for Precision Systems, Inc. on August 14, 2019. Classification: No Action Indicated (NAI).

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Record Information

Company

Precision Systems, Inc.

Inspection Date

August 14, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f73b2106-d6bd-440f-90a3-6e5518294ce1

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