# FDA Inspection 1262841 - Zimmer Biomet CMF and Thoracic LLC - March 04, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/zimmer-biomet-cmf-and-thoracic-llc/121ba5cb-95a3-4ce8-868e-1dadda9d48cd
Source feed: FDA_Inspections

> FDA Inspection 1262841 for Zimmer Biomet CMF and Thoracic LLC on March 04, 2025. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1262841
- Company Name: Zimmer Biomet CMF and Thoracic LLC
- Inspection Date: 2025-03-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Florida District Office

## Related Documents

- [FDA Inspection 1262841 - 2025-03-04](https://www.globalkeysolutions.net/records/fda_inspections/zimmer-biomet-cmf-and-thoracic-llc/1d421f15-c252-41ab-bee1-48951744295d)
- [FDA Inspection 1024178 - 2017-09-01](https://www.globalkeysolutions.net/records/fda_inspections/zimmer-biomet-cmf-and-thoracic-llc/32b85659-722b-490d-9af1-39ed27e0cb39)
- [FDA Inspection 1024178 - 2017-09-01](https://www.globalkeysolutions.net/records/fda_inspections/zimmer-biomet-cmf-and-thoracic-llc/e64816ed-aed4-40f9-a41a-e87ea09a2b07)
- [FDA Inspection 947565 - 2015-10-30](https://www.globalkeysolutions.net/records/fda_inspections/zimmer-biomet-cmf-and-thoracic-llc/ad58128b-8204-42b4-b03f-e86c938e0993)
- [FDA Inspection 947565 - 2015-10-30](https://www.globalkeysolutions.net/records/fda_inspections/zimmer-biomet-cmf-and-thoracic-llc/daa5ee4a-f77f-42b8-9919-c2cdcdf9ad8f)

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

Office: https://www.globalkeysolutions.net/offices/florida-district-office/95b2a118-0b78-46e0-a54c-982bd7ce51c9
