# Zimmer Biomet CMF and Thoracic LLC – FDA Inspection, May 24, 2018

Source: https://www.keypedia.com/records/fda_inspections/zimmer-biomet-cmf-and-thoracic-llc/72ed293c-e977-4942-9003-1d7ce2b7c511
Source feed: FDA_Inspections

> FDA inspection 1053122 of Zimmer Biomet CMF and Thoracic LLC, May 24, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 803. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1053122
- Company Name: Zimmer Biomet CMF and Thoracic LLC
- Inspection Date: 2018-05-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1262841 - 2025-03-04](https://www.keypedia.com/records/fda_inspections/zimmer-biomet-cmf-and-thoracic-llc/1d421f15-c252-41ab-bee1-48951744295d)
- [FDA Inspection 1024178 - 2017-09-01](https://www.keypedia.com/records/fda_inspections/zimmer-biomet-cmf-and-thoracic-llc/e64816ed-aed4-40f9-a41a-e87ea09a2b07)
- FDA Inspection 947565 - 2015-10-30
- FDA Inspection 764538 - 2012-01-17

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nabil-nakhoul/d676e9c9-566c-4e59-84e8-1dc474e4e48d)

Company: https://www.keypedia.com/companies/zimmer-biomet-cmf-and-thoracic-llc/7bb07ce7-8968-4ce2-935a-9d851d6dee0e

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