§ 809.20. General requirements for manufacturers and producers of in vitro diagnostic products.
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/us/cfr/t21/s§ 809.20·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
(a)[Reserved]
(b)Compliance with good manufacturing practices. In vitro diagnostic products shall be manufactured in accordance with the good manufacturing practices requirements found in part 820 of this chapter and, if applicable, with § 610.44 of this chapter. [41 FR 6903, Feb. 13, 1976, as amended at 42 FR 42530, Aug. 23, 1977; 43 FR 31527, July 21, 1978; 66 FR 31165, June 11, 2001]
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§ 809.20
General requirements for manufacturers and producers of in vitro diagnostic products.
Fed. Reg.×3
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