Bausch & Lomb, Incorporated
FDA inspection history in Lynchburg, Virginia, 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 Lynchburg, Virginia.
Cited most
Across all Bausch & Lomb, Incorporated observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.90(a)Nonconforming product1
The complete Bausch & Lomb, Incorporated file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Lynchburg, Virginia
One Form 483 · 2018 · 2 observations
Latest: Form 483, Jul 13, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-07-13 | 483 Form 483 | Lynchburg, Virginia | 2 | $99 |
Investigators on these documents
FEI number 1000305478 · most recent document Jul 13, 2018
About Bausch & Lomb, Incorporated
How many FDA Form 483s has Bausch & Lomb, Incorporated received?
FDA Intel has 1 Form 483 on file for Bausch & Lomb, Incorporated; the most recent is dated Jul 13, 2018.
When was Bausch & Lomb, Incorporated last inspected by FDA?
The most recent FDA inspection document on file for Bausch & Lomb, Incorporated is a Form 483 dated Jul 13, 2018, for the site in Lynchburg, Virginia.
What did FDA cite at Bausch & Lomb, Incorporated?
The regulations cited most in the observations on file for Bausch & Lomb, Incorporated are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.90(a) (Nonconforming product), 1 time.