Haleon US Holdings LLC
FDA inspection history in East Durham, New York, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at East Durham, New York.
Cited most
Across all Haleon US Holdings observations on file
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Haleon US Holdings file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
East Durham, New York
One Form 483 · 2018 · 2 observations
Latest: Form 483, Sep 11, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-09-11 | 483 Form 483 | East Durham, New York | 2 | $99 |
Investigators on these documents
FEI number 1314819 · most recent document Sep 11, 2018
About Haleon US Holdings LLC
How many FDA Form 483s has Haleon US Holdings LLC received?
FDA Intel has 1 Form 483 on file for Haleon US Holdings LLC; the most recent is dated Sep 11, 2018.
When was Haleon US Holdings LLC last inspected by FDA?
The most recent FDA inspection document on file for Haleon US Holdings LLC is a Form 483 dated Sep 11, 2018, for the site in East Durham, New York.
What did FDA cite at Haleon US Holdings LLC?
The regulations cited most in the observations on file for Haleon US Holdings LLC are 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.