Alcon Laboratories Ireland, Ltd
FDA inspection history in Cork, Ireland, 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 Cork, Ireland.
Cited most
Across all Alcon Laboratories Ireland observations on file
- 21 CFR 803.50If I am a manufacturer, what reporting requirements apply to me?1
The complete Alcon Laboratories Ireland file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Cork, Ireland
One Form 483 · 2015 · 1 observation
Latest: Form 483, Jan 15, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-01-15 | 483 Form 483 | Cork, Ireland | 1 | $99 |
Investigators on these documents
FEI number 3002808262 · most recent document Jan 15, 2015
About Alcon Laboratories Ireland, Ltd
How many FDA Form 483s has Alcon Laboratories Ireland, Ltd received?
FDA Intel has 1 Form 483 on file for Alcon Laboratories Ireland, Ltd; the most recent is dated Jan 15, 2015.
When was Alcon Laboratories Ireland, Ltd last inspected by FDA?
The most recent FDA inspection document on file for Alcon Laboratories Ireland, Ltd is a Form 483 dated Jan 15, 2015, for the site in Cork, Ireland.
What did FDA cite at Alcon Laboratories Ireland, Ltd?
The regulations cited most in the observations on file for Alcon Laboratories Ireland, Ltd are 21 CFR 803.50 (If I am a manufacturer, what reporting requirements apply to me?), 1 time.