Manufacturers of certain devices during a public health emergency are required to notify the FDA of an interruption or permanent discontinuance in manufacturing of such devices by Section 506J of the FD & C Act.

Manufacturers of certain devices during a public health emergency are required to notify the FDA of an interruption or permanent discontinuance in manufacturing of such devices by Section 506J of the FD&C Act.

Source: Food and Drug Adminstration (FDA): CDRHNew - May 6, 2020 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news