FDA Inspection 1266113 - Leltek Inc. - March 06, 2025

FDA Inspection 1266113 for Leltek Inc. on March 06, 2025. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 1266113 for Leltek Inc. on March 06, 2025. Classification: Official Action Indicated (OAI).

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Record Information

Company

Leltek Inc.

Inspection Date

March 6, 2025

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: dfee7b16-d3a5-4da5-b763-0335a83e9bc8

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