The FDA and FTC have recently issued warning letters to 7 companies for selling fraudulent COVID-19 products.
What this means to you:
The FDA has classified the products in question as unapproved or illegal products. There are corrective actions to be taken and prioritized.
These warning letters can be alarming and are a matter of public record under FOIA. The most important thing is to act immediately, reach out for help, and implement the remediation and going forward process solutions that make sense.
The Compliance Insight Team