BioVectra Inc.
FDA inspection history in Charlottetown, Canada, 2017 to 2024
- 3
- Form 483s
Every document, by year
- Form 483
2017: one Form 483; 2022: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Charlottetown, Canada.
- 2022–24Two Form 483s, at Charlottetown, Canada.
- 2024The longest 483 on file: 2 observations over 2 pages at Charlottetown, Canada.
Cited most
Across all BioVectra observations on file
- 21 CFR 211.180General requirements2
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.160General requirements1
The complete BioVectra 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
Charlottetown, Canada
Three Form 483s · 2017 to 2024 · 5 observations
Latest: Form 483, Apr 19, 2024 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-04-19 | 483 Form 483 | Charlottetown, Canada | 2 | $99 |
| 2022-08-26 | 483 Form 483 | Charlottetown, Canada | 2 | $99 |
| 2017-02-17 | 483 Form 483 | Charlottetown, Canada | 1 | $99 |
Investigators on these documents
FEI number 3004063541 · most recent document Apr 19, 2024
About BioVectra Inc.
How many FDA Form 483s has BioVectra Inc. received?
FDA Intel has 3 Form 483s on file for BioVectra Inc.; the most recent is dated Apr 19, 2024.
When was BioVectra Inc. last inspected by FDA?
The most recent FDA inspection document on file for BioVectra Inc. is a Form 483 dated Apr 19, 2024, for the site in Charlottetown, Canada.
What did FDA cite at BioVectra Inc.?
The regulations cited most in the observations on file for BioVectra Inc. are 21 CFR 211.180 (General requirements), 2 times; 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.160 (General requirements), 1 time.