Company
United StatesCovidien, LLC, Minneapolis, MN – FDA Inspections
Inspection records and compliance data for Covidien, LLC in Minneapolis, Minnesota. 3 FDA inspections on record, 1 Form 483, last inspected September 22, 2017.
Company Profile
This profile covers Covidien, LLC based in Minneapolis, Minnesota, United States.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 0
- NAI
- 3
- Form 483s
- 1
- Warning letters
- 0
First inspected February 26, 2010. Last inspected September 22, 2017.
Most cited issue areas
- DHR content1 inspection
- Lack of or inadequate process validation1 inspection
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| September 22, 2017 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1026123 |
| October 17, 2012 | NAI | Medical Devices & Rad Health · Compliance: Devices | 803358 |
| February 26, 2010 | NAI | Medical Devices & Rad Health · Compliance: Devices | 648649 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
Covidien, LLC
FEI Number
3004962788
Address
161 Cheshire Ln N Ste 100, Minneapolis, Minnesota 55441, United States
Country
United States
ID: 7880d213-f3b7-4a04-9fa1-9f0d32cc7f4c