FDA Inspection 1148524 - Litex Manufacturing, Inc - August 05, 2021

FDA Inspection 1148524 for Litex Manufacturing, Inc on August 05, 2021. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1148524 for Litex Manufacturing, Inc on August 05, 2021. Classification: No Action Indicated (NAI).

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Record Information

Company

Litex Manufacturing, Inc

Inspection Date

August 5, 2021

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f7f94bac-991e-4b8a-8a07-1cddde1c6074

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