Reporting- Waiver Request Requirements For An Owner or Operator, If Use By Electronic Means for Submission of Registration & Listing Information Is Not Reasonable ( One time burden)
Implementation of Sections 222, 223 and 224 of the Food and Drug Administration Act of 2007
OMB: 0910-0625
IC ID: 193002
⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0625 can be found here: