Description:
America First Legal (AFL) filed a Freedom of Information Act (FOIA) request with the U.S. Department of Health and Human Services (HHS) and the U.S. Food and Drug Administration (FDA) to obtain records relating to the suppression of Ivermectin to treat COVID-19 by federal government bureaucrats.Documents:
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 14th Interim Production
Type: Agency Record
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 14th Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 13th Interim Production
Type: Agency Record
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 13th Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 12th Interim Production
Type: Agency Record
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 12th Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 11th Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 10th Interim Production
Type: Agency Record
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 10th Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 9th Interim Production
Type: Agency Record
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 9th Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 8th Interim Production Part 2
Type: Agency Record
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 8th Interim Production Part 1
Type: Agency Record
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 8th Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 7th Interim Production
Type: Agency Record
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 7th Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 6th Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 5th Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 4th Interim Response/Production
Type: Interim Agency Response/Agency Record
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 3rd Interim Production
Type: Agency Record
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 3rd Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 2nd Interim Production
Type: Agency Record
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 2nd Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 1st Interim Production
Type: Agency Record
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – 1st Interim Response
Type: Interim Agency Response
Ivermectin COVID-19 Suppression – Food and Drug Administration (FDA) – Acknowledgment Letter
Type: Acknowledgment Letter
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – Acknowledgment Letter
Type: Acknowledgment Letter
Ivermectin COVID-19 Suppression – Food and Drug Administration (FDA) – Confirmation Letter
Type: Confirmation Letter
Ivermectin COVID-19 Suppression – Department of Health and Human Services (HHS) – FOIA Letter
Type: FOIA Letter
Ivermectin COVID-19 Suppression – Food and Drug Administration (FDA) – FOIA Letter
Type: FOIA Letter
