Medicap Laboratories
FDA inspection history in Toronto, Canada, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Toronto, Canada.
Cited most
Across all Medicap Laboratories observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.63Equipment design, size, and location1
- 21 CFR 211.67Equipment cleaning and maintenance1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Medicap Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Toronto, Canada
One Form 483 · 2019 · 5 observations
Latest: Form 483, Jun 14, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-06-14 | 483 Form 483 | Toronto, Canada | 5 | $99 |
FEI number 3006370451 · most recent document Jun 14, 2019
About Medicap Laboratories
How many FDA Form 483s has Medicap Laboratories received?
FDA Intel has 1 Form 483 on file for Medicap Laboratories; the most recent is dated Jun 14, 2019.
When was Medicap Laboratories last inspected by FDA?
The most recent FDA inspection document on file for Medicap Laboratories is a Form 483 dated Jun 14, 2019, for the site in Toronto, Canada.
What did FDA cite at Medicap Laboratories?
The regulations cited most in the observations on file for Medicap Laboratories are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.63 (Equipment design, size, and location), 1 time.