Mayo Clinic Pharmacy
FDA inspection history across 2 sites, 2018
- 1
- Response
- 1
- Form 483
Every document, by year
- Response
- Form 483
2018: one 483 response and one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One 483 response and one Form 483, at Minnesota and Rochester, Minnesota.
Cited most
Across all Mayo Clinic Pharmacy observations on file
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.167Special testing requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Mayo Clinic Pharmacy file.
All 2 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
Minnesota
One 483 response · 2018
Latest: Response, Aug 30, 2018 →Rochester, Minnesota
One Form 483 · 2018 · 5 observations
Latest: Form 483, Aug 15, 2018 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-08-30 | Response 483 response | Minnesota | — | $199 |
| 2018-08-15 | 483 Form 483 | Rochester, Minnesota | 5 | $99 |
Investigators on these documents
FEI number 3005070479 · most recent document Aug 30, 2018
About Mayo Clinic Pharmacy
How many FDA Form 483s has Mayo Clinic Pharmacy received?
FDA Intel has 1 Form 483 on file for Mayo Clinic Pharmacy; the most recent is dated Aug 15, 2018.
When was Mayo Clinic Pharmacy last inspected by FDA?
The most recent FDA inspection document on file for Mayo Clinic Pharmacy is a Form 483 dated Aug 15, 2018, for the site in Rochester, Minnesota.
What did FDA cite at Mayo Clinic Pharmacy?
The regulations cited most in the observations on file for Mayo Clinic Pharmacy are 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.167 (Special testing requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.