Medtronic, Inc.
483 response sent September 9, 2011 · Minneapolis, Minnesota
- Inspection
- Nov 17, 2010 – Jan 21, 2011
- Investigators
- Jessica L. Johnson· Susan M. Atcher
- Pages
- 3
- FEI number
- 3007566237
In short: This is Medtronic, Inc.'s written response to FDA, dated September 9, 2011, for its site in Minneapolis, Minnesota (FEI 3007566237). It sets out the corrective actions the firm committed to.
Inside this response
This inspection in context
Jessica L. Johnson
7 documents · 2011–2013
Cites 820.30 (design controls) more than any other section. Most of their documents are for sites in Minnesota.
The firmMedtronic, Inc. history
All 5 documents on file for this site, in date order, with what was cited at each inspection.
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Questions about this response
Who inspected Medtronic, Inc.?
Jessica L. Johnson and Susan M. Atcher are named on this 483 response, for the inspection of Nov 17, 2010 – Jan 21, 2011. Each investigator has a profile showing what they cite most.
When was Medtronic, Inc. inspected by FDA?
The inspection ran Nov 17, 2010 – Jan 21, 2011, and the 483 response is dated September 9, 2011.
How do I get the full 483 response for Medtronic, Inc.?
Download the original PDF from FDA Intel for $199, with no subscription. You also get an invoice PDF with the order.