# FDA Inspection 1030015 - Cima Technology Inc - October 27, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/cima-technology-inc/2c58c8a9-fe22-4630-8ad3-735e1d29c376
Source feed: FDA_Inspections

> FDA Inspection 1030015 for Cima Technology Inc on October 27, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030015
- Company Name: Cima Technology Inc
- Inspection Date: 2017-10-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1030015 - 2017-10-27](https://www.globalkeysolutions.net/records/fda_inspections/cima-technology-inc/92740d0d-3c4f-42bc-9234-f0761f3b9be1)
- [FDA Inspection 898476 - 2014-10-07](https://www.globalkeysolutions.net/records/fda_inspections/cima-technology-inc/92426e58-d14f-47a7-a7ae-33f439677baa)
- [FDA Inspection 898476 - 2014-10-07](https://www.globalkeysolutions.net/records/fda_inspections/cima-technology-inc/dd2bd878-0cfa-4df0-929a-9d3334bcf9c8)
- [FDA Inspection 855486 - 2013-11-12](https://www.globalkeysolutions.net/records/fda_inspections/cima-technology-inc/5ad12a95-e2a6-4212-9dff-651351379d70)
- [FDA Inspection 752988 - 2011-11-09](https://www.globalkeysolutions.net/records/fda_inspections/cima-technology-inc/a71d579a-1a4e-4861-b6bc-04e5b58ef6cd)

Company: https://www.globalkeysolutions.net/companies/cima-technology-inc/257e7e02-ddb5-421e-8f8a-20f4e0dc2200

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