SI Group, Inc.
FDA inspection history in Orangeburg, South Carolina, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Orangeburg, South Carolina.
Cited most
Across all SI Group observations on file
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.42Design and construction features1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete SI Group file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Orangeburg, South Carolina
One Form 483 · 2025
Latest: Form 483, Jan 17, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-01-17 | 483 Form 483 | Orangeburg, South Carolina | — | $99 |
FEI number 3011012288 · most recent document Jan 17, 2025
About SI Group, Inc.
How many FDA Form 483s has SI Group, Inc. received?
FDA Intel has 1 Form 483 on file for SI Group, Inc.; the most recent is dated Jan 17, 2025.
When was SI Group, Inc. last inspected by FDA?
The most recent FDA inspection document on file for SI Group, Inc. is a Form 483 dated Jan 17, 2025, for the site in Orangeburg, South Carolina.
What did FDA cite at SI Group, Inc.?
The regulations cited most in the observations on file for SI Group, Inc. are 21 CFR 211.188 (Batch production and control records), 1 time; 21 CFR 211.42 (Design and construction features), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.