L M Manufacturing Limited
FDA inspection history in Northampton, United Kingdom, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Northampton, United Kingdom.
Cited most
Across all L M Manufacturing Limited observations on file
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.165Testing and release for distribution1
The complete L M Manufacturing Limited file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Northampton, United Kingdom
One Form 483 · 2022 · 2 observations
Latest: Form 483, Feb 2, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-02-02 | 483 Form 483 | Northampton, United Kingdom | 2 | $99 |
Investigators on these documents
FEI number 3015337531 · most recent document Feb 2, 2022
About L M Manufacturing Limited
How many FDA Form 483s has L M Manufacturing Limited received?
FDA Intel has 1 Form 483 on file for L M Manufacturing Limited; the most recent is dated Feb 2, 2022.
When was L M Manufacturing Limited last inspected by FDA?
The most recent FDA inspection document on file for L M Manufacturing Limited is a Form 483 dated Feb 2, 2022, for the site in Northampton, United Kingdom.
What did FDA cite at L M Manufacturing Limited?
The regulations cited most in the observations on file for L M Manufacturing Limited are 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.165 (Testing and release for distribution), 1 time.