Analytical laboratories records shall include:
- A. name of substance;
- B. the form or forms in which substance is received, imported or manufactured and the concentration of the substance;
- C. quantity and strength received;
- D. date of receipt;
- E. name and DEA registry number of supplier;
- F. adequate record of distribution.
[16.19.20.35 NMAC - Rp 16.19.20.35 NMAC, 6/26/2018]