FDA Inspection
Covidien, LLCCovidien, LLC – FDA Inspection, May 10, 2017
Record Details
This FDA Inspection record concerns Covidien, LLC, with an inspection on May 10, 2017, issued by the San Francisco District Office, covering medical devices & rad health.
- Company
- Covidien, LLC
- Inspection Date
- May 10, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 1c6ebb5d-e51c-409b-ab14-8e464a882551
Inspection Facts
- Inspection number
- 1031445
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Covidien, LLC
9| Date | Classification | Office | Project area |
|---|---|---|---|
| September 20, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 3, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 16, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 17, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 5, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Covidien, LLC
- FDA Inspection 984992 - 2016-09-20
- FDA Inspection 932211 - 2015-06-03
- FDA Inspection 834276 - 2013-05-16
- FDA Inspection 782057 - 2012-05-17
- FDA Inspection 756849 - 2011-12-05
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