# Autocam Medical Devices, LLC – FDA Inspection, Oct 22, 2025

Source: https://www.keypedia.com/records/fda_inspections/autocam-medical-devices-llc/eb421261-3e53-4566-a61e-8cd387bb8005
Source feed: FDA_Inspections

> FDA inspection 1290184 of Autocam Medical Devices, LLC, October 22, 2025. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1290184
- Company Name: Autocam Medical Devices, LLC
- Inspection Date: 2025-10-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: New England District Office
- Citation Count: 3

## Related Documents

- FDA Inspection 1055436 - 2018-05-18

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/sunita-pandey/008e5bb8-0eb3-45d8-8524-734ac0454250)

Company: https://www.keypedia.com/companies/autocam-medical-devices-llc/93881644-ef58-4b9e-950b-e451c3e4b398

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144