Data catalog
CFR sections cited by the FDA
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Continuing the CFR sections cited by the FDA list, 1000 records per page, after 820.30(h).
- 820.30(i)§ 820.30 Design controls.
- 820.30(j)§ 820.30 Design controls.
- 820.35(a)
- 820.35(b)
- 820.35(c)
- 820.40§ 820.40 Document controls.
- 820.40(a)§ 820.40 Document controls.
- 820.40(b)§ 820.40 Document controls.
- 820.45(b)
- 820.50§ 820.50 Purchasing controls.
- 820.50(a)§ 820.50 Purchasing controls.
- 820.50(a)(1)§ 820.50 Purchasing controls.
- 820.50(a)(2)§ 820.50 Purchasing controls.
- 820.50(a)(3)§ 820.50 Purchasing controls.
- 820.50(b)§ 820.50 Purchasing controls.
- 820.60§ 820.60 Identification.
- 820.65§ 820.65 Traceability.
- 820.70(a)§ 820.70 Production and process controls.
- 820.70(a)(1)§ 820.70 Production and process controls.
- 820.70(a)(2)§ 820.70 Production and process controls.
- 820.70(a)(3)§ 820.70 Production and process controls.
- 820.70(a)(4)§ 820.70 Production and process controls.
- 820.70(a)(5)§ 820.70 Production and process controls.
- 820.70(b)§ 820.70 Production and process controls.
- 820.70(c)§ 820.70 Production and process controls.
- 820.70(d)§ 820.70 Production and process controls.
- 820.70(e)§ 820.70 Production and process controls.
- 820.70(f)§ 820.70 Production and process controls.
- 820.70(g)§ 820.70 Production and process controls.
- 820.70(g)(1)§ 820.70 Production and process controls.
- 820.70(g)(2)§ 820.70 Production and process controls.
- 820.70(g)(3)§ 820.70 Production and process controls.
- 820.70(h)§ 820.70 Production and process controls.
- 820.70(i)§ 820.70 Production and process controls.
- 820.72(a)§ 820.72 Inspection, measuring, and test equipment.
- 820.72(a)(1)
- 820.72(b)§ 820.72 Inspection, measuring, and test equipment.
- 820.72(b)(1)§ 820.72 Inspection, measuring, and test equipment.
- 820.72(b)(2)§ 820.72 Inspection, measuring, and test equipment.
- 820.75(a)§ 820.75 Process validation.
- 820.75(b)§ 820.75 Process validation.
- 820.75(b)(1)§ 820.75 Process validation.
- 820.75(b)(2)§ 820.75 Process validation.
- 820.75(c)§ 820.75 Process validation.
- 820.80(a)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(b)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(c)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(d)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(d)(1)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(d)(2)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(d)(3)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(d)(4)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(e)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(e)(1)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(e)(2)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(e)(3)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(e)(4)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.80(e)(5)§ 820.80 Receiving, in-process, and finished device acceptance.
- 820.86§ 820.86 Acceptance status.
- 820.90(a)§ 820.90 Nonconforming product.
- 820.90(b)(1)§ 820.90 Nonconforming product.
- 820.90(b)(2)§ 820.90 Nonconforming product.
- 821.20(a)§ 821.20 Devices subject to tracking.
- 821.25(a)§ 821.25 Device tracking system and content requirements: manufacturer requirements.
- 821.25(b)§ 821.25 Device tracking system and content requirements: manufacturer requirements.
- 821.25(c)§ 821.25 Device tracking system and content requirements: manufacturer requirements.
- 821.25(c)(1)§ 821.25 Device tracking system and content requirements: manufacturer requirements.
- 821.25(c)(3)§ 821.25 Device tracking system and content requirements: manufacturer requirements.
- 821.25(d)§ 821.25 Device tracking system and content requirements: manufacturer requirements.
- 821.30(a)§ 821.30 Tracking obligations of persons other than device manufacturers: distributor…
- 821.50(a)§ 821.50 Availability.
- 830.300(a)§ 830.300 Devices subject to device identification data submission requirements.
- 830.310(b)§ 830.310 Information required for unique device identification.
- 830.320(a)§ 830.320 Submission of unique device identification information.
- 860.7(g)(1)§ 860.7 Determination of safety and effectiveness.
- 860.7(g)(2)§ 860.7 Determination of safety and effectiveness.
About this dataset
Title 21 of the Code of Federal Regulations contains the FDA's regulations, including current good manufacturing practice and quality system requirements that inspections cite.
Source: U.S. Code of Federal Regulations (eCFR); citation statistics from FDA inspection and warning-letter data