# Covidien, LLC – FDA Inspection, Sep 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/covidien-llc/9f03a8cd-678a-473a-ad48-01338fcb14ca
Source feed: FDA_Inspections

> FDA inspection 1026123 of Covidien, LLC, September 22, 2017. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026123
- Company Name: Covidien, LLC
- Inspection Date: 2017-09-22
- 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: 2

## Related Documents

- FDA Inspection 803358 - 2012-10-17
- FDA Inspection 648649 - 2010-02-26

## Related Officers

- [Company Rep](https://www.keypedia.com/people/susan-m-matthias/cd23c465-4411-4988-8676-2089e265622a)

Company: https://www.keypedia.com/companies/covidien-llc/7880d213-f3b7-4a04-9fa1-9f0d32cc7f4c

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