What did the FDA find wrong with Moy-Fincher Medical Group?

The FDA issued a warning letter citing labeling violations related to their products or manufacturing practices.

Are Moy-Fincher Medical Group products safe to use?

Based on the FDA's findings, consumers should exercise caution. The company was found to have labeling violations that may affect product safety.

What should I do if I've used Moy-Fincher Medical Group products?

If you have used products from Moy-Fincher Medical Group and experience any adverse effects, contact your healthcare provider immediately. You can also report adverse events to the FDA's MedWatch program.

Moy-Fincher Medical Group FDA Warning (2018)

Name: Moy-Fincher Medical Group FDA Warning (2018)
Creator: Supplement Safety Data Team
Published: 2026-03-27T01:44:25.173603

Compiled by the Supplement Safety Data Team | Sourced from Official FDA Records on February 08, 2018

MODERATE SEVERITY 2018

Disclaimer: This report is an analysis of a public FDA warning letter. It is not medical advice. If you have consumed these products and feel unwell, contact a healthcare professional immediately.

Executive Summary

The FDA issued a warning letter to Moy-Fincher Medical Group on February 08, 2018 citing labeling violations. The letter was issued by the FDA.

Labeling Violations

Detailed Analysis

False Claims and Regulatory Violations

The FDA identified regulatory violations in Moy-Fincher Medical Group's operations or product claims.

Potential Health Risks

Consumers should be aware of potential risks associated with products from Moy-Fincher Medical Group.

Regulatory Context

The Food and Drug Administration has completed an evaluation of your firm 's corrective actions in response to our Warning Letter #440852 issued February 12, 2015. Based on our evaluation, it appears that you have addressed the violation(s) contained in this Warning Letter. Future FDA inspections and regulatory activities will further assess the adequacy and sustainability of these corrections.

This letter does not relieve you or your firm from the responsibility of taking all necessary steps to assure sustained compliance with the Federal Food, Drug, and Cosmetic Act and its implementing regulations or with other relevant legal authority. The Agency expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This Jetter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means.

Latasha A. RobinsonBranch ChiefDietary Supplements & Labeling Assessment BranchOffice of ComplianceCenter for Food Safetyand Applied Nutrition

Key Entities Identified

Moy-Fincher Medical Group FDA Warning Letter

Frequently Asked Questions

What did the FDA find wrong with Moy-Fincher Medical Group?: The FDA issued a warning letter citing labeling violations related to their products or manufacturing practices.
Are Moy-Fincher Medical Group products safe to use?: Based on the FDA's findings, consumers should exercise caution. The company was found to have labeling violations that may affect product safety.
What should I do if I've used Moy-Fincher Medical Group products?: If you have used products from Moy-Fincher Medical Group and experience any adverse effects, contact your healthcare provider immediately. You can also report adverse events to the FDA's MedWatch program.

Source Document

This report is based on an official FDA warning letter. The original document is a public record.

View Original FDA Warning Letter

Medical Disclaimer: This report is an analysis of public FDA warning letters. It is not medical advice. If you have consumed these products and feel unwell, contact a healthcare professional immediately. You can report adverse events to the FDA MedWatch program.