# Covidien LP – FDA Inspection, May 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/covidien-lp/2cd73d82-0751-4cdf-ab11-aa9dbe00beb6
Source feed: FDA_Inspections

> FDA inspection 1029477 of Covidien LP, May 19, 2017. Form 483 issued. 9 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029477
- Company Name: Covidien LP
- Inspection Date: 2017-05-19
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: New England District Office
- Citation Count: 0

## Related Documents

- [FDA Inspection 1191674 - 2022-11-18](https://www.keypedia.com/records/fda_inspections/covidien-lp/7e2d98c2-fd64-42ed-82b0-cfc26c4e55e5)
- [FDA Inspection 1034600 - 2017-05-17](https://www.keypedia.com/records/fda_inspections/covidien-lp/fbb361f2-41fa-4eb9-b6a2-342d752b0763)
- [FDA Inspection 844859 - 2013-08-15](https://www.keypedia.com/records/fda_inspections/covidien-lp/a65b1270-3133-4887-a0d1-e3fdc4324bb1)
- FDA Inspection 792561 - 2012-07-20
- FDA Inspection 778312 - 2012-04-09

Company: https://www.keypedia.com/companies/covidien-lp/63d22b1b-1374-4530-ab2d-48293cfaee75

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144