21 CFR Subpart C
Requirements for Manufacturers and Producers
June 25, 2020
§
809.20
General requirements for manufacturers and producers of in vitro diagnostic products
§
809.30
Restrictions on the sale, distribution and use of analyte specific reagents
§
809.40
Restrictions on the sale, distribution, and use of OTC test sample collection systems for drugs of abuse testing
Tried the LawStack mobile app?
Join thousands and try LawStack mobile for FREE today.
- Carry the law offline, wherever you go.
- Download CFR, USC, rules, and state law to your mobile device.
