# Covidien, LLC – FDA Inspection, Sep 2, 2010

Source: https://www.keypedia.com/records/fda_inspections/covidien-llc/69470360-cd68-4817-a2ff-5332153c19a1
Source feed: FDA_Inspections

> FDA inspection 681613 of Covidien, LLC, September 02, 2010. Classification: No Action Indicated (NAI). 9 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 681613
- Company Name: Covidien, LLC
- Inspection Date: 2010-09-02
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1031445 - 2017-05-10](https://www.keypedia.com/records/fda_inspections/covidien-llc/1c6ebb5d-e51c-409b-ab14-8e464a882551)
- FDA Inspection 984992 - 2016-09-20
- FDA Inspection 932211 - 2015-06-03
- FDA Inspection 834276 - 2013-05-16
- FDA Inspection 782057 - 2012-05-17

Company: https://www.keypedia.com/companies/covidien-llc/0787a7fa-505a-419e-afe8-8c492f5cf1d8

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7