GlaxoSmithKline Consumer Healthcare
FDA inspection history in Aiken, South Carolina, 2015
- 1
- Form 483
Every document, by year
- Form 483
2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Aiken, South Carolina.
Cited most
Across all GlaxoSmithKline Consumer Healthcare observations on file
- 21 CFR 211.142Warehousing procedures1
- 21 CFR 211.198(b)(2)Complaint files1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.56(b)Sanitation1
The complete GlaxoSmithKline Consumer Healthcare file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Aiken, South Carolina
One Form 483 · 2015 · 4 observations
Latest: Form 483, Jul 10, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-07-10 | 483 Form 483 | Aiken, South Carolina | 4 | $99 |
Investigators on these documents
FEI number 1046838 · most recent document Jul 10, 2015
About GlaxoSmithKline Consumer Healthcare
How many FDA Form 483s has GlaxoSmithKline Consumer Healthcare received?
FDA Intel has 1 Form 483 on file for GlaxoSmithKline Consumer Healthcare; the most recent is dated Jul 10, 2015.
When was GlaxoSmithKline Consumer Healthcare last inspected by FDA?
The most recent FDA inspection document on file for GlaxoSmithKline Consumer Healthcare is a Form 483 dated Jul 10, 2015, for the site in Aiken, South Carolina.
What did FDA cite at GlaxoSmithKline Consumer Healthcare?
The regulations cited most in the observations on file for GlaxoSmithKline Consumer Healthcare are 21 CFR 211.142 (Warehousing procedures), 1 time; 21 CFR 211.198(b)(2) (Complaint files), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.