CFR section

21 CFR 225.130: Equipment

PART 225-CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS · Subpart F-Facilities and Equipment

Key facts

Citation 21 CFR 225.130
Section Equipment
Part PART 225-CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS
Subpart Subpart F-Facilities and Equipment
Subchapter 21 CFR C Drugs General
Product types cited Drugs, Veterinary
Regulation text (excerpt) Equipment shall be capable of producing a medicated feed of intended potency and purity, and shall be maintained in a reasonably clean and orderly manner. Scales and liquid metering devices shall be accurate and of suitable size, design, construction, precision, and accuracy for their intended purposes. All equipment shall be designed, constructed, installed, and maintained so as to facilitate inspection and use of cleanout procedure(s).

At a glance

  • 10–99 Inspections citing this section
  • 1–9 Warning letters citing this section

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About CFR sections cited by the FDA

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

Browse all CFR sections cited by the FDA