Medtronic, Inc.
FDA inspection history in Minneapolis, Minnesota, 2011
- 4
- Responses
- 1
- Form 483
Every document, by year
- Response
- Form 483
2011: four 483 responses and one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2011Four 483 responses and one Form 483, at Minneapolis, Minnesota.
Cited most
Across all Medtronic observations on file
- 21 CFR 820.30Design controls2
- 21 CFR 820.100Corrective and preventive action1
- 21 CFR 820.198Complaint files1
- 21 CFR 820.75Process validation1
The complete Medtronic file.
All 5 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
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Sites
Minneapolis, Minnesota
Four 483 responses and one Form 483 · 2011 · 5 observations
Latest: Response, Sep 9, 2011 →
Documents
5 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2011-09-09 | Response 483 response | Minneapolis, Minnesota | — | $199 |
| 2011-07-15 | Response 483 response | Minneapolis, Minnesota | — | $199 |
| 2011-05-13 | Response 483 response | Minneapolis, Minnesota | — | $199 |
| 2011-03-25 | Response 483 response | Minneapolis, Minnesota | — | $199 |
| 2011-01-21 | 483 Form 483 | Minneapolis, Minnesota | 5 | $99 |
Investigators on these documents
FEI number 3007566237 · most recent document Sep 9, 2011
About Medtronic, Inc.
How many FDA Form 483s has Medtronic, Inc. received?
FDA Intel has 1 Form 483 on file for Medtronic, Inc.; the most recent is dated Jan 21, 2011.
When was Medtronic, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Medtronic, Inc. is a Form 483 dated Jan 21, 2011, for the site in Minneapolis, Minnesota.
What did FDA cite at Medtronic, Inc.?
The regulations cited most in the observations on file for Medtronic, Inc. are 21 CFR 820.30 (Design controls), 2 times; 21 CFR 820.100 (Corrective and preventive action), 1 time; 21 CFR 820.198 (Complaint files), 1 time.