FDA Inspection
Covidien LPCovidien LP – FDA Inspection, May 19, 2017
Record Details
This FDA Inspection record concerns Covidien LP, with an inspection on May 19, 2017, issued by the New England District Office, covering medical devices & rad health.
- Company
- Covidien LP
- Inspection Date
- May 19, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 2cd73d82-0751-4cdf-ab11-aa9dbe00beb6
Inspection Facts
- Inspection number
- 1029477
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Covidien LP
9| Date | Classification | Office | Project area |
|---|---|---|---|
| November 18, 2022 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 17, 2017 | Not classified | New England District Office | |
| August 15, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 20, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 9, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Covidien LP
- FDA Inspection 1191674 - 2022-11-18
- FDA Inspection 1034600 - 2017-05-17
- FDA Inspection 844859 - 2013-08-15
- FDA Inspection 792561 - 2012-07-20
- FDA Inspection 778312 - 2012-04-09
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