At the present time, all COVID medical products offered under the auspices of a “vaccine” are granted approval as an Emergency Use Authorization.

They are not approved by the FDA.

Mandating investigational or experimental therapies is therefore unlawful according to 21 U.S.C. §360bbb-3 “Authorization for medical products for use in emergencies”.

If your organization is mandating this, it is violating Federal Law & this action will be held accountable.

Learn the facts: https://www.americasfrontlinedoctors.org/legal/vaccines-the-law