Warning letterPosted November 18, 2025
FDA warning letter to Siddha Flower Essences, LLC., dba Siddha Remedies
CGMP/Finished Pharmaceuticals/Adulterated
FDA posted a warning letter to Siddha Flower Essences, LLC., dba Siddha Remedies on November 18, 2025; the letter is dated November 4, 2025. Subject: CGMP/Finished Pharmaceuticals/Adulterated. Issuing office: Center for Drug Evaluation and Research (CDER).
On the record
- Company
- Siddha Flower Essences, LLC., dba Siddha Remedies
- Subject
- CGMP/Finished Pharmaceuticals/Adulterated
- Issuing office
- Center for Drug Evaluation and Research (CDER)
- Letter dated
- 2025-11-04
- Posted by FDA
- 2025-11-18
- Source
- FDA warning letters ↗
CFR cited
The record cites 10 sections of 21 CFR Parts 207, 210 and 211.
The full record
An account shows the violations FDA described and each CFR section it cited.
What a warning letter is
A warning letter is FDA's notice to a company that it found significant violations of federal requirements. FDA asks for a written response, normally within 15 working days. The letter is advisory: it states the agency's position and is not a final agency action.
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From FDA warning letters. The record may have changed since it was read.
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