# Zimmer Biomet CMF and Thoracic LLC – FDA Inspection, Sep 1, 2017

Source: https://www.keypedia.com/records/fda_inspections/zimmer-biomet-cmf-and-thoracic-llc/e64816ed-aed4-40f9-a41a-e87ea09a2b07
Source feed: FDA_Inspections

> FDA inspection 1024178 of Zimmer Biomet CMF and Thoracic LLC, September 01, 2017. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1024178
- Company Name: Zimmer Biomet CMF and Thoracic LLC
- Inspection Date: 2017-09-01
- 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: 3

## 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 1053122 - 2018-05-24](https://www.keypedia.com/records/fda_inspections/zimmer-biomet-cmf-and-thoracic-llc/72ed293c-e977-4942-9003-1d7ce2b7c511)
- FDA Inspection 947565 - 2015-10-30
- FDA Inspection 764538 - 2012-01-17

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/richard-k-vogel/3ddd8bff-24fd-40ee-b0a7-fb5333a520f5)

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