AMENDED 483
FDA AMENDED_483 - Unknown Company - July 22, 2019
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Record Details
This AMENDED 483 record concerns null, with an inspection on July 22, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- July 22, 2019
- Product Type
- Devices
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ID · 00b89fb1-0164-4be5-af2d-d02897700198
Violation Codes1
21 CFR 210
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