# ZIMMER BIOMET dba Embody, Inc. – FDA Inspection, Aug 18, 2023

Source: https://www.keypedia.com/records/fda_inspections/zimmer-biomet-dba-embody-inc/d7ba3d40-a97e-454d-9449-3ab576eb0def
Source feed: FDA_Inspections

> FDA inspection 1216962 of ZIMMER BIOMET dba Embody, Inc., August 18, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1216962
- Company Name: ZIMMER BIOMET dba Embody, Inc.
- Inspection Date: 2023-08-18
- 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: 2

## Related Officers

- [Tiki Dixon](https://www.keypedia.com/people/tiki-dixon/b3160a2c-ef16-4fa2-b9b9-4c3a0ed17c5b)

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