GlaxoSmithKline
FDA inspection history in Conshohocken, Pennsylvania, 2018 to 2024
- 2
- Form 483s
Every document, by year
- Form 483
2018: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Conshohocken, Pennsylvania.
- 2024One Form 483, at Conshohocken, Pennsylvania.
- 2024The longest 483 on file: 5 observations over 6 pages at Conshohocken, Pennsylvania.
Cited most
Across all GlaxoSmithKline observations on file
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.42Design and construction features1
The complete GlaxoSmithKline 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
Conshohocken, Pennsylvania
Two Form 483s · 2018 to 2024 · 7 observations
Latest: Form 483, Sep 25, 2024 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-09-25 | 483 Form 483 | Conshohocken, Pennsylvania | 5 | $99 |
| 2018-01-26 | 483 Form 483 | Conshohocken, Pennsylvania | 2 | $99 |
Investigators on these documents
Anita R. Mfoh (1)Jun Liu (1)Priscilla Amaral (1)Yi Wang (1)Zhen Ren (1)Zhong Li (1)
FEI number 3004055938 · most recent document Sep 25, 2024
About GlaxoSmithKline
How many FDA Form 483s has GlaxoSmithKline received?
FDA Intel has 2 Form 483s on file for GlaxoSmithKline; the most recent is dated Sep 25, 2024.
When was GlaxoSmithKline last inspected by FDA?
The most recent FDA inspection document on file for GlaxoSmithKline is a Form 483 dated Sep 25, 2024, for the site in Conshohocken, Pennsylvania.
What did FDA cite at GlaxoSmithKline?
The regulations cited most in the observations on file for GlaxoSmithKline are 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.160 (General requirements), 1 time.