FDA 483 - R. N. Eaton & Company, Inc. - March 02, 2022

R. N. Easton & Co Inc, a manufacturer in Riverside, MO, was cited for deficiencies in drug product testing and release during an FDA inspection. The firm failed to verify alcohol content in finished product hand sanitizer and did not test the active ingredient ethanol for methanol content prior to distribution. These issues indicate a significant lapse in quality control for drug product release.