At TEQ, we are dedicated to assuring our customers the highest quality production of their packaging.
According to the U.S. Food and Drug Administration (FDA), being FDA registered means:
Most establishments that are required to register with the FDA are also required to list the devices that are made there and the activities that are performed on those devices. If a device requires premarket approval or notification before being marketed in the U.S., then the owner/operator should also provide the FDA premarket submission number (510(k), PMA, PDP, HDE).
