Notice: Official Public Record
PT Shimasse Prata Citra FDA Warning (2018)
Compiled by the Supplement Safety Data Team | Sourced from Official FDA Records on January 09, 2018
MODERATE SEVERITY
Center for Food Safety and Applied Nutrition 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 PT Shimasse Prata Citra on January 09, 2018 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 Shimasse Prata Citra's operations or product claims.
Potential Health Risks
Consumers should be aware of potential risks associated with products from PT Shimasse Prata Citra.
Regulatory Context
This warning letter is part of the FDA's enforcement of federal regulations.
Key Entities Identified
PT Shimasse Prata Citra FDA Warning Letter
Frequently Asked Questions
- What did the FDA find wrong with PT Shimasse Prata Citra?
- The FDA issued a warning letter citing regulatory violations related to their products or manufacturing practices.
- Are PT Shimasse Prata Citra 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 Shimasse Prata Citra products?
- If you have used products from PT Shimasse Prata Citra 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.