# Southeastern Technology Inc. dba Autocam Medical - Inspection Records

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

> Inspection records and compliance data for Southeastern Technology Inc. dba Autocam Medical in Murfreesboro, Tennessee. Access full analysis and detailed observations.

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## Details

- Name: Southeastern Technology Inc. dba Autocam Medical
- FEI Number: 1000221916
- City: Murfreesboro
- State: Tennessee
- Country Name: United States
- Address Line 1: 905 Industrial Dr
- Zip Code: 37129

## Related Documents

- [FDA Inspection 1222746 - Southeastern Technology Inc. dba Autocam Medical - 2023-11-09](https://www.keypedia.com/records/fda_inspections/southeastern-technology-inc-dba-autocam-medical/e18c74d0-3ff2-47d4-8c78-08cc639ee00e) — classification: No Action Indicated (NAI), source: FDA, date: November 9, 2023
- [FDA Inspection 1222746 - Southeastern Technology Inc. dba Autocam Medical - 2023-11-09](https://www.keypedia.com/records/fda_inspections/southeastern-technology-inc-dba-autocam-medical/20f82020-1309-4f0f-a6c1-8794f028b667) — classification: No Action Indicated (NAI), source: FDA, date: November 9, 2023
- [FDA Inspection 1123232 - Southeastern Technology Inc. dba Autocam Medical - 2020-03-04](https://www.keypedia.com/records/fda_inspections/southeastern-technology-inc-dba-autocam-medical/bdb428bf-34da-4622-9434-2868c1a000b8) — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2020
- [FDA Inspection 1007448 - Southeastern Technology Inc. dba Autocam Medical - 2017-04-07](https://www.keypedia.com/records/fda_inspections/southeastern-technology-inc-dba-autocam-medical/a6e34f5e-1bd2-471a-832f-8d6397ff05b9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 7, 2017
- [FDA Inspection 716913 - Southeastern Technology Inc. dba Autocam Medical - 2011-03-22](https://www.keypedia.com/records/fda_inspections/southeastern-technology-inc-dba-autocam-medical/9882e759-b7ef-4bad-92bd-775d95384a1c) — classification: No Action Indicated (NAI), source: FDA, date: March 22, 2011

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