Sheffield Pharmaceuticals LLC
FDA inspection history in New London, Connecticut, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at New London, Connecticut.
Cited most
Across all Sheffield Pharmaceuticals observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.30(i)Design controls1
- 21 CFR 820.40Document controls1
- 21 CFR 820.70(g)(1)Production and process controls1
The complete Sheffield Pharmaceuticals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
New London, Connecticut
One Form 483 · 2019 · 7 observations
Latest: Form 483, Mar 15, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-03-15 | 483 Form 483 | New London, Connecticut | 7 | $99 |
Investigators on these documents
FEI number 1210513 · most recent document Mar 15, 2019
About Sheffield Pharmaceuticals LLC
How many FDA Form 483s has Sheffield Pharmaceuticals LLC received?
FDA Intel has 1 Form 483 on file for Sheffield Pharmaceuticals LLC; the most recent is dated Mar 15, 2019.
When was Sheffield Pharmaceuticals LLC last inspected by FDA?
The most recent FDA inspection document on file for Sheffield Pharmaceuticals LLC is a Form 483 dated Mar 15, 2019, for the site in New London, Connecticut.
What did FDA cite at Sheffield Pharmaceuticals LLC?
The regulations cited most in the observations on file for Sheffield Pharmaceuticals LLC are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time; 21 CFR 820.30(i) (Design controls), 1 time.