As specified in 21 CFR 1.235(b), the cancellation for a facility’s registration must include the following information:
• The facility’s registration number;
• Whether the facility is domestic or foreign;
• The facility name and address;
• The name, address, and email address (if available) of the individual submitting the cancellation;
• For registration cancellations not submitted by the owner, operator, or agent in charge of the facility, the email address of the individual who authorized submission of the registration cancellation, unless FDA has granted a waiver under 21 CFR 1.245; and
• A statement certifying that the information submitted is true and accurate, and that the person submitting the cancellation is authorized by the facility to cancel its registration.
