Company
United StatesCovidien, Boulder, CO – FDA Inspections
Inspection records and compliance data for Covidien in Boulder, Colorado. 4 FDA inspections on record, last inspected July 16, 2025.
Company Profile
This profile covers Covidien based in Boulder, Colorado, United States.
FDA Inspection History
- FDA inspections
- 4
- OAI
- 0
- VAI
- 0
- NAI
- 3
- Unclassified
- 1
- Form 483s
- 0
- Warning letters
- 0
First inspected January 13, 2010. Last inspected July 16, 2025.
FDA inspections (4)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| July 16, 2025 | Not classified | Medical Devices & Rad Health | 1260161 |
| February 26, 2015 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 917680 |
| April 22, 2010 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 659164 |
| January 13, 2010 | NAI | Medical Devices & Rad Health · Compliance: Devices | 639004 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
Covidien
FEI Number
2936999
Address
6135 Gunbarrel Ave, Boulder, Colorado 80301, United States
Country
United States
ID: e6412dbd-2a1d-4e1c-83d3-1de260dda259