# FDA Inspection 965801 - Allpro, Inc. - April 05, 2016

Source: https://www.keypedia.com/records/fda_inspections/allpro-inc/b751419f-e560-4780-b238-0cdc6915901d
Source feed: FDA_Inspections

> FDA Inspection 965801 for Allpro, Inc. on April 05, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 965801
- Company Name: Allpro, Inc.
- Inspection Date: 2016-04-05
- 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 965801 - 2016-04-05](https://www.keypedia.com/records/fda_inspections/allpro-inc/29a4244a-0aae-4a89-9bd7-d8f33926c57c)

Company: https://www.keypedia.com/companies/allpro-inc/5dbc716c-a809-4896-a963-8979b8b31c1c

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