FDA Advisory No. 2020-497 || DISTRIBUTION OF FDA APPROVED COVID-19 RAPID ANTIBODY TEST KITS

The Food and Drug Administration (FDA) reiterates to all licensed importer/distributor that COVID-19 test kits is strictly for use of medical professional use and not intended for personal use.

The product should be strictly distributed to appropriate establishments or institutions. Subsequently, this should be acquired by the general public through a prescription from a licensed physician. The administration of the test must be performed by a doctor or a trained health professional. Furthermore, the interpretation of results must be done by a doctor.

Attachment:-> FDA Advisory No.2020-497

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