GC Hanford Manufacturing Company
FDA inspection history in Syracuse, New York, 2022 to 2025
- 2
- Form 483s
Every document, by year
- Form 483
2022: one Form 483; 2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Syracuse, New York.
- 2025One Form 483, at Syracuse, New York.
- 2025The longest 483 on file: 6 observations over 6 pages at Syracuse, New York.
Cited most
Across all GC Hanford Manufacturing observations on file
- 21 CFR 211.22(d)Responsibilities of quality control unit2
- 21 CFR 211.42(c)(10)(i)Design and construction features2
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.56(a)Sanitation1
- 21 CFR 211.63Equipment design, size, and location1
The complete GC Hanford Manufacturing 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
Syracuse, New York
Two Form 483s · 2022 to 2025 · 9 observations
Latest: Form 483, Mar 20, 2025 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-03-20 | 483 Form 483 | Syracuse, New York | 6 | $99 |
| 2022-06-17 | 483 Form 483 | Syracuse, New York | 3 | $99 |
Investigators on these documents
FEI number 1310197 · most recent document Mar 20, 2025
About GC Hanford Manufacturing Company
How many FDA Form 483s has GC Hanford Manufacturing Company received?
FDA Intel has 2 Form 483s on file for GC Hanford Manufacturing Company; the most recent is dated Mar 20, 2025.
When was GC Hanford Manufacturing Company last inspected by FDA?
The most recent FDA inspection document on file for GC Hanford Manufacturing Company is a Form 483 dated Mar 20, 2025, for the site in Syracuse, New York.
What did FDA cite at GC Hanford Manufacturing Company?
The regulations cited most in the observations on file for GC Hanford Manufacturing Company are 21 CFR 211.22(d) (Responsibilities of quality control unit), 2 times; 21 CFR 211.42(c)(10)(i) (Design and construction features), 2 times; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time.