OIRA Conclusion of EO 12866 Regulatory Review
| RIN: 0910-AF27 View EO 12866 Meetings | Received Date: 04/11/2013 |
| Title: Infant Formula: Current Good Manufacturing Practices; Quality Control Procedures; Notification Requirements; Records and Reports; and Quality Factors | |
| Agency/Subagency: HHS / FDA | Stage: Final Rule |
| Concluded Action: Consistent with Change | Concluded Date: 12/20/2013 |
| Legal Deadline: None | Economically Significant: No |
| Publication Date: 02/10/2014 | Unfunded Mandates: No |
| Major: No | Related To Homeland Security: No |
| Regulatory Flexibility Analysis Required: Yes | Small Entities Affected: Businesses |
| Federalism Implications: No | Affordable Care Act [Pub. L. 111-148 & 111-152]: No |
| International Impacts: Yes | Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]: No |
| Pandemic Response: Uncollected | |
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