# Southeastern Technology Inc. dba Autocam Medical – FDA Inspection, Apr 7, 2017

Source: https://www.keypedia.com/records/fda_inspections/southeastern-technology-inc-dba-autocam-medical/a6e34f5e-1bd2-471a-832f-8d6397ff05b9
Source feed: FDA_Inspections

> FDA inspection 1007448 of Southeastern Technology Inc. dba Autocam Medical, April 07, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1007448
- Company Name: Southeastern Technology Inc. dba Autocam Medical
- Inspection Date: 2017-04-07
- 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 Documents

- [FDA Inspection 1222746 - 2023-11-09](https://www.keypedia.com/records/fda_inspections/southeastern-technology-inc-dba-autocam-medical/e18c74d0-3ff2-47d4-8c78-08cc639ee00e)
- FDA Inspection 1123232 - 2020-03-04
- FDA Inspection 716913 - 2011-03-22

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/southeastern-technology-inc-dba-autocam-medical/e58af7b1-4110-496e-af44-54e0c403c3ff

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