# FDA Inspection 959800 - Integra Microfrance - February 18, 2016

Source: https://www.keypedia.com/records/fda_inspections/integra-microfrance/22888e33-6a81-4179-a6b1-a21c21dc2eb7
Source feed: FDA_Inspections

> FDA Inspection 959800 for Integra Microfrance on February 18, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 959800
- Company Name: Integra Microfrance
- Inspection Date: 2016-02-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 857175 - 2013-09-12](https://www.keypedia.com/records/fda_inspections/integra-microfrance/ca4fdb80-5199-4f32-8e0b-7bd503b68102)

Company: https://www.keypedia.com/companies/integra-microfrance/463d96a9-7bc2-4340-8fd4-dde99b72d466

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