# FDA Inspection 919491 - MIM Software Inc - March 27, 2015

Source: https://www.keypedia.com/records/fda_inspections/mim-software-inc/1ddd85f2-8737-487f-b77d-d6905173878e
Source feed: FDA_Inspections

> FDA Inspection 919491 for MIM Software Inc on March 27, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 919491
- Company Name: MIM Software Inc
- Inspection Date: 2015-03-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 919491 - 2015-03-27](https://www.keypedia.com/records/fda_inspections/mim-software-inc/3b902144-effd-4cd0-9f20-83d961054311)
- [FDA Inspection 742239 - 2011-09-02](https://www.keypedia.com/records/fda_inspections/mim-software-inc/fa0a85b7-1354-4b2f-8a57-4549df9f19af)

Company: https://www.keypedia.com/companies/mim-software-inc/a3fa6387-bb71-4f3c-929b-69ebfcc04bb1

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