Avasol LLC
FDA inspection history in Santa Barbara, California, 2023 to 2025
- 2
- Form 483s
Every document, by year
- Form 483
2023: one Form 483; 2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023–25Two Form 483s, at Santa Barbara, California.
- 2023The longest 483 on file: 7 observations over 5 pages at Santa Barbara, California.
Cited most
Across all Avasol observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.160(b)(4)General requirements1
- 21 CFR 211.166(b)Stability testing1
- 21 CFR 211.182Equipment cleaning and use log1
- 21 CFR 211.186(a)Master production and control records1
The complete Avasol 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
Santa Barbara, California
Two Form 483s · 2023 to 2025 · 11 observations
Latest: Form 483, Feb 12, 2025 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-02-12 | 483 Form 483 | Santa Barbara, California | 4 | $99 |
| 2023-11-09 | 483 Form 483 | Santa Barbara, California | 7 | $99 |
Investigators on these documents
FEI number 3014630458 · most recent document Feb 12, 2025
About Avasol LLC
How many FDA Form 483s has Avasol LLC received?
FDA Intel has 2 Form 483s on file for Avasol LLC; the most recent is dated Feb 12, 2025.
When was Avasol LLC last inspected by FDA?
The most recent FDA inspection document on file for Avasol LLC is a Form 483 dated Feb 12, 2025, for the site in Santa Barbara, California.
What did FDA cite at Avasol LLC?
The regulations cited most in the observations on file for Avasol LLC are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.160(b)(4) (General requirements), 1 time; 21 CFR 211.166(b) (Stability testing), 1 time.