Solesence, Inc.
FDA inspection history in Romeoville, Illinois, 2023 to 2026
- 2
- Form 483s
Every document, by year
- Form 483
2023: one Form 483; 2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Romeoville, Illinois.
- 2023The longest 483 on file: 2 observations over 3 pages at Romeoville, Illinois.
- 2026One Form 483, at Romeoville, Illinois.
Cited most
Across all Solesence observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures1
The complete Solesence 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
Romeoville, Illinois
Two Form 483s · 2023 to 2026 · 3 observations
Latest: Form 483, Jan 9, 2026 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-01-09 | 483 Form 483 | Romeoville, Illinois | 1 | $99 |
| 2023-04-13 | 483 Form 483 | Romeoville, Illinois | 2 | $99 |
Investigators on these documents
FEI number 3003574860 · most recent document Jan 9, 2026
About Solesence, Inc.
How many FDA Form 483s has Solesence, Inc. received?
FDA Intel has 2 Form 483s on file for Solesence, Inc.; the most recent is dated Jan 9, 2026.
When was Solesence, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Solesence, Inc. is a Form 483 dated Jan 9, 2026, for the site in Romeoville, Illinois.
What did FDA cite at Solesence, Inc.?
The regulations cited most in the observations on file for Solesence, Inc. are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.