# Ameditech Inc - Inspection Records

Source: https://www.keypedia.com/companies/ameditech-inc/86ad904f-34ad-4313-917a-5692f0b0513c

> Inspection records and compliance data for Ameditech Inc in San Diego, California. Access full analysis and detailed observations.

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## Details

- Name: Ameditech Inc
- FEI Number: 3003789989
- City: San Diego
- State: California
- Country Name: United States
- Address Line 1: 9940 Mesa Rim Rd
- Zip Code: 92121

## Related Documents

- [FDA Inspection 1236951 - Ameditech Inc - 2024-08-16](https://www.keypedia.com/records/fda_inspections/ameditech-inc/f0436be1-12e5-409e-8ee3-3cfe77992271) — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2024
- [FDA Inspection 1236951 - Ameditech Inc - 2024-08-16](https://www.keypedia.com/records/fda_inspections/ameditech-inc/024df255-8812-4ea5-873c-e233c6d75a09) — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2024
- [FDA Inspection 970516 - Ameditech Inc - 2016-05-12](https://www.keypedia.com/records/fda_inspections/ameditech-inc/031518be-9315-4c33-821c-57bf4198306d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 12, 2016
- [FDA Inspection 970516 - Ameditech Inc - 2016-05-12](https://www.keypedia.com/records/fda_inspections/ameditech-inc/c85a9615-6378-4a8e-a4d2-f49ee4cabffd) — classification: No Action Indicated (NAI), source: FDA, date: May 12, 2016
- [FDA Inspection 728406 - Ameditech Inc - 2011-05-26](https://www.keypedia.com/records/fda_inspections/ameditech-inc/015f7e97-2213-4133-87f6-83d82e7561f6) — classification: No Action Indicated (NAI), source: FDA, date: May 26, 2011
- [FDA Inspection 728406 - Ameditech Inc - 2011-05-26](https://www.keypedia.com/records/fda_inspections/ameditech-inc/c17c7685-f4a6-48fe-9511-adaf0495babb) — classification: No Action Indicated (NAI), source: FDA, date: May 26, 2011
- [FDA Inspection 681628 - Ameditech Inc - 2010-09-23](https://www.keypedia.com/records/fda_inspections/ameditech-inc/5533832f-601f-47ac-bc90-ee5b508ff1ff) — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2010

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