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# Comments Sought on Device Accredited Person Inspections
- URL: https://www.fdaweb.com/comments-sought-on-device-accredited-person-inspections/
- Published: 2017-11-21T12:00:00.000Z
- Updated: 2026-09-14T23:02:55.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5140180

*Federal Register* notice: FDA is seeking comments on an information collection extension for its guidance on “Notification of the Intent To Use an Accredited Person Under the Accredited Persons Inspection Program OMB Control Number 0910-0569.” The voluntary third-party inspection program is applicable to manufacturers of Class 2 or 3 medical devices that meet certain eligibility criteria. FDA estimates that about 10 device makers user the accredited person program annually. To view the notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2017-11-21/pdf/2017-25158.pdf?ref=fdaweb.com).