FDA 21 CFR Part 895 Banned Devices

FDA 21 CFR Part 895 Banned Devices:

FDA 21 CFR Part 895 Banned Devices: This part describes the procedures by which the FDA Commissioner may institute proceedings to make a device intended for human use that presents substantial deception or an unreasonable and substantial risk of illness or injury a banned device.

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FDA 21 CFR Part 895 Banned Devices:

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