10508. INSPECTION OF ESTABLISHMENT REGISTRATION AND DEVICE LISTING

10508 INSPECTION OF ESTABLISHMENT REGISTRATION AND DEVICE LISTING 10508.1 A copy of the forms FDA-2891 that the registrant files shall be available for inspection at the Department. Upon request, verification of registration number or location of a registered establishment shall be provided. 10508.2 The following information filed under the device listing requirements will be available for public disclosure: (a) Each form FDA-2892 or its Department equivalent submitted; (b) All labels submitted; (c) All labeling submitted; (d) All advertisements submitted; and (e) All data or information that has already become a matter of public knowledge. 10508.3 Requests for device listing information identified in § 10508.2 of this section shall be directed to the Department. 10508.4 Requests for device listing information not identified in § 10508.2 shall be submitted and handled as specified in these regulations. SOURCE: Final Rulemaking published at 60 DCR 10252 (July 12, 2013). District of Columbia Municipal Regulations Public Health and Medicine 22-B DCMR § 10508