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PT. Nusantara Jaya Abadi FDA Warning (2017)

Compiled by the Supplement Safety Data Team | Sourced from Official FDA Records on December 29, 2017

MODERATE SEVERITY Center for Food Safety and Applied Nutrition 2017
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 PT. Nusantara Jaya Abadi on December 29, 2017 citing regulatory violations. The letter was issued by Center for Food Safety and Applied Nutrition.

Regulatory Violations

Detailed Analysis

False Claims and Regulatory Violations

The FDA identified regulatory violations in PT. Nusantara Jaya Abadi's operations or product claims.

Potential Health Risks

Consumers should be aware of potential risks associated with products from PT. Nusantara Jaya Abadi.

Regulatory Context

This warning letter is part of the FDA's enforcement of federal regulations.

Key Entities Identified

PT. Nusantara Jaya Abadi FDA Warning Letter

Frequently Asked Questions

What did the FDA find wrong with PT. Nusantara Jaya Abadi?
The FDA issued a warning letter citing regulatory violations related to their products or manufacturing practices.
Are PT. Nusantara Jaya Abadi products safe to use?
Based on the FDA's findings, consumers should exercise caution. The company was found to have regulatory issues that may affect product safety.
What should I do if I've used PT. Nusantara Jaya Abadi products?
If you have used products from PT. Nusantara Jaya Abadi 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.