21 CFR Part 1210: Regulations Under the Federal Import Milk Act
Part 1210 of title 21 runs to 23 sections across 4 subparts, and sits in subchapter L, Regulations Under Certain Other Acts Administered by the Food and Drug Administration. Every section is reproduced in full and is current to 2026-09-10.
- Sections
- 23
- Subparts
- 4
- Words of regulation
- 1,803
- Current to
- 2026-09-10
Subpart A: General Provisions
Subpart B: Inspection and Testing
- 1210.10 Availability for examination and inspection1
- 1210.11 Sanitary inspection of dairy farms1
- 1210.12 Physical examination of cows2
- 1210.13 Tuberculin test2
- 1210.14 Sanitary inspection of plants1
- 1210.15 Pasteurization; equipment and methods1
- 1210.16 Method of bacterial count1
- 1210.17 Authority to sample and inspect1
- 1210.18 Scoring1
Subpart C: Permit Control
- 1210.20 Application for permit1
- 1210.21 Permit number1
- 1210.22 Form of tag1
- 1210.23 Permits granted on certificates1
- 1210.24 Temporary permits1
- 1210.25 Permits for pasteurized milk or cream1
- 1210.26 Permits for raw milk or cream1
- 1210.27 Permits waiving clauses 2 and 5, section 2 of the Federal Import Milk Act1
- 1210.28 Permits waiving clause 4, section 2 of the Federal Import Milk Act1
Subpart D: Hearings
Read 21 CFR part 1210 at the eCFR · All of 21 CFR for food safety
Questions
- What does 21 CFR part 1210 cover?
- 21 CFR part 1210 is Regulations Under the Federal Import Milk Act. It runs to 23 sections across 4 subparts and sits in subchapter L of chapter I, Regulations Under Certain Other Acts Administered by the Food and Drug Administration.
Every section of part 1210 is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.