# FDA Inspection 867311 - Calimex USA Corporation - February 24, 2014

Source: https://www.keypedia.com/records/fda_inspections/calimex-usa-corporation/ab6d74d9-d6f4-4e0d-b959-db764d12b70f
Source feed: FDA_Inspections

> FDA Inspection 867311 for Calimex USA Corporation on February 24, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 867311
- Company Name: Calimex USA Corporation
- Inspection Date: 2014-02-24
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 867311 - 2014-02-24](https://www.keypedia.com/records/fda_inspections/calimex-usa-corporation/1506000c-4fdd-44ba-b0a4-5cb387bd64a1)
- [FDA Inspection 832426 - 2013-05-22](https://www.keypedia.com/records/fda_inspections/calimex-usa-corporation/3bf211d6-67be-4761-bafc-2cdd7c75b50c)
- [FDA Inspection 832426 - 2013-05-22](https://www.keypedia.com/records/fda_inspections/calimex-usa-corporation/327dbf76-397b-4397-a6b6-a1380efcdfce)

Company: https://www.keypedia.com/companies/calimex-usa-corporation/0e143df3-6e30-419b-84b3-a2a6d5d8e394

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