# FDA Inspection 804101 - Memometal Technologies - September 26, 2012

Source: https://www.keypedia.com/records/fda_inspections/memometal-technologies/b1c7ba3d-cf6f-42a0-b18f-937c679a4521
Source feed: FDA_Inspections

> FDA Inspection 804101 for Memometal Technologies on September 26, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 804101
- Company Name: Memometal Technologies
- Inspection Date: 2012-09-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 804101 - 2012-09-26](https://www.keypedia.com/records/fda_inspections/memometal-technologies/3778a951-0959-4ede-92bb-5b4105966457)
- [FDA Inspection 629445 - 2009-10-01](https://www.keypedia.com/records/fda_inspections/memometal-technologies/9aa15228-5ce8-4d6d-a95e-127ea24bf690)

Company: https://www.keypedia.com/companies/memometal-technologies/56538040-95d6-4ad2-bfff-28a3b5ef52b5

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