# Cima Technology Inc – FDA Inspection, Oct 27, 2017

Source: https://www.keypedia.com/records/fda_inspections/cima-technology-inc/92740d0d-3c4f-42bc-9234-f0761f3b9be1
Source feed: FDA_Inspections

> FDA inspection 1030015 of Cima Technology Inc, October 27, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. Form 483 issued. 4 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 898476 - 2014-10-07](https://www.keypedia.com/records/fda_inspections/cima-technology-inc/dd2bd878-0cfa-4df0-929a-9d3334bcf9c8)
- [FDA Inspection 855486 - 2013-11-12](https://www.keypedia.com/records/fda_inspections/cima-technology-inc/5ad12a95-e2a6-4212-9dff-651351379d70)
- FDA Inspection 752988 - 2011-11-09
- FDA Inspection 664661 - 2010-06-02

## Related Officers

- [Company Rep](https://www.keypedia.com/people/dennis-r-hock/f13e2db1-b808-466d-a974-e5af2d5dfdb0)

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

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