Bio Products Laboratory Ltd
FDA inspection history in Elstree, 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 Elstree, United Kingdom.
Cited most
Across all Bio Products Laboratory observations on file
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.160General requirements1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.192Production record review1
The complete Bio Products Laboratory file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Elstree, United Kingdom
One Form 483 · 2022 · 7 observations
Latest: Form 483, Aug 30, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-08-30 | 483 Form 483 | Elstree, United Kingdom | 7 | $99 |
Investigators on these documents
FEI number 1000184635 · most recent document Aug 30, 2022
About Bio Products Laboratory Ltd
How many FDA Form 483s has Bio Products Laboratory Ltd received?
FDA Intel has 1 Form 483 on file for Bio Products Laboratory Ltd; the most recent is dated Aug 30, 2022.
When was Bio Products Laboratory Ltd last inspected by FDA?
The most recent FDA inspection document on file for Bio Products Laboratory Ltd is a Form 483 dated Aug 30, 2022, for the site in Elstree, United Kingdom.
What did FDA cite at Bio Products Laboratory Ltd?
The regulations cited most in the observations on file for Bio Products Laboratory Ltd are 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.160 (General requirements), 1 time.