# FDA Inspection 1216962 - ZIMMER BIOMET dba Embody, Inc. - August 18, 2023

Source: https://www.keypedia.com/records/fda_inspections/zimmer-biomet-dba-embody-inc/24ffb477-723a-4ea1-9eb4-ebcc519538e3
Source feed: FDA_Inspections

> FDA Inspection 1216962 for ZIMMER BIOMET dba Embody, Inc. on August 18, 2023. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1216962
- Company Name: ZIMMER BIOMET dba Embody, Inc.
- Inspection Date: 2023-08-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1216962 - 2023-08-18](https://www.keypedia.com/records/fda_inspections/zimmer-biomet-dba-embody-inc/d7ba3d40-a97e-454d-9449-3ab576eb0def)

Company: https://www.keypedia.com/companies/zimmer-biomet-dba-embody-inc/d89d4aaa-b169-4ede-a2c6-7d26a9bb4d16

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