Siddha Flower Essences LLC
FDA inspection history in Oxnard, California, 2018 to 2025
- 1
- Warning letter
- 1
- Form 483
Every document, by year
- Warning letter
- Form 483
2018: one Form 483; 2025: one warning letter.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Oxnard, California.
- 2025One warning letter, at Oxnard, California.
Cited most
Across all Siddha Flower Essences observations on file
- 21 CFR 211.84(d)(1)Testing and approval or rejection of components, drug product containers, and closures2
- 21 CFR 211.180(e)(2)General requirements1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.25(a)Personnel qualifications1
The complete Siddha Flower Essences file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Oxnard, California
One warning letter and one Form 483 · 2018 to 2025 · 6 observations
Latest: Warning letter, Nov 4, 2025 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-11-04 | Warning letter Warning letter | Oxnard, California | — | $99 |
| 2018-12-12 | 483 Form 483 | Oxnard, California | 6 | $99 |
Investigators on these documents
FEI number 3014145088 · most recent document Nov 4, 2025
About Siddha Flower Essences LLC
How many FDA Form 483s has Siddha Flower Essences LLC received?
FDA Intel has 1 Form 483 on file for Siddha Flower Essences LLC; the most recent is dated Dec 12, 2018.
When was Siddha Flower Essences LLC last inspected by FDA?
The most recent FDA inspection document on file for Siddha Flower Essences LLC is a Form 483 dated Dec 12, 2018, for the site in Oxnard, California.
What did FDA cite at Siddha Flower Essences LLC?
The regulations cited most in the observations on file for Siddha Flower Essences LLC are 21 CFR 211.84(d)(1) (Testing and approval or rejection of components, drug product containers, and closures), 2 times; 21 CFR 211.180(e)(2) (General requirements), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.
Has Siddha Flower Essences LLC received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Siddha Flower Essences LLC; the most recent is dated Nov 4, 2025.