Bioreliance Ltd.
FDA inspection history in Glasgow, United Kingdom, 2016 to 2019
- 3
- Form 483s
Every document, by year
- Form 483
2016: one Form 483; 2019: two Form 483s.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Glasgow, United Kingdom.
- 2016The longest 483 on file: 17 observations over 7 pages at Glasgow, United Kingdom.
- 2019Two Form 483s, at Glasgow, United Kingdom.
Cited most
Across all Bioreliance observations on file
- 21 CFR 211.113Control of microbiological contamination5
- 21 CFR 211.67Equipment cleaning and maintenance5
- 21 CFR 211.160General requirements4
- 21 CFR 211.192Production record review4
- 21 CFR 211.188Batch production and control records2
The complete Bioreliance file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Glasgow, United Kingdom
Three Form 483s · 2016 to 2019 · 28 observations
Latest: Form 483, Sep 27, 2019 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-09-27 | 483 Form 483 | Glasgow, United Kingdom | 3 | $99 |
| 2019-03-15 | 483 Form 483 | Glasgow, United Kingdom | 8 | $99 |
| 2016-03-23 | 483 Form 483 | Glasgow, United Kingdom | 17 | $99 |
Investigators on these documents
FEI number 3005343934 · most recent document Sep 27, 2019
About Bioreliance Ltd.
How many FDA Form 483s has Bioreliance Ltd. received?
FDA Intel has 3 Form 483s on file for Bioreliance Ltd.; the most recent is dated Sep 27, 2019.
When was Bioreliance Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Bioreliance Ltd. is a Form 483 dated Sep 27, 2019, for the site in Glasgow, United Kingdom.
What did FDA cite at Bioreliance Ltd.?
The regulations cited most in the observations on file for Bioreliance Ltd. are 21 CFR 211.113 (Control of microbiological contamination), 5 times; 21 CFR 211.67 (Equipment cleaning and maintenance), 5 times; 21 CFR 211.160 (General requirements), 4 times.