All our programs include routine maintenance that includes quality assurance inspections by our factory-trained technicians. These inspections are performed and designed to follow the guidelines set forth by the Food and Drug Administration (FDA), and other government and industry initiatives.

Publicom, Inc. is a registered Device Establishment with the U. S. Department of Health and Human Services, Food and Drug Administration as authorized by Section 510 of the Food, Drug and Cosmetic Act (21 U.S.C 360).

All our products are covered by our
48-hour emergency call response
should a unit malfunction.

To request immediate service, support or technical information, contact us.