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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter A - General |
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Part 7 - Enforcement Policy |
| Subpart A - General Provisions |
| § 7.1 - Scope. |
| § 7.3 - Definitions. |
| § 7.12 - Guaranty. |
| § 7.13 - Suggested forms of guaranty. |
| Subpart B - XXX |
| Subpart C - Recalls (Including Product Corrections)—Guidance on Policy, Procedures, and Industry Responsibilities |
| § 7.40 - Recall policy. |
| § 7.41 - Health hazard evaluation and recall classification. |
| § 7.42 - Recall strategy. |
| § 7.45 - Food and Drug Administration-requested recall. |
| § 7.46 - Firm-initiated recall. |
| § 7.49 - Recall communications. |
| § 7.50 - Public notification of recall. |
| § 7.53 - Recall status reports. |
| § 7.55 - Termination of a recall. |
| § 7.59 - General industry guidance. |
| Subpart D - XXX |
| Subpart E - Criminal Violations |
| § 7.84 - Opportunity for presentation of views before report of criminal violation. |
| § 7.85 - Conduct of a presentation of views before report of criminal violation. |
| § 7.87 - Records related to opportunities for presentation of views conducted before report of criminal violation. |