# FDA Inspection 981034 - Neotract  Inc - June 08, 2016

Source: https://www.keypedia.com/records/fda_inspections/neotract-inc/7e5bb615-7edd-473e-9feb-65a799e9cdad
Source feed: FDA_Inspections

> FDA Inspection 981034 for Neotract  Inc on June 08, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 981034
- Company Name: Neotract  Inc
- Inspection Date: 2016-06-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 981034 - 2016-06-08](https://www.keypedia.com/records/fda_inspections/neotract-inc/811811f5-6237-4be8-84b6-a3dd681c4319)
- [FDA Inspection 871509 - 2014-02-27](https://www.keypedia.com/records/fda_inspections/neotract-inc/45476ff0-e9e6-4c42-9174-6869851dc8ef)
- [FDA Inspection 871509 - 2014-02-27](https://www.keypedia.com/records/fda_inspections/neotract-inc/badd7f5f-520c-4ae6-b081-9c233df79b39)

Company: https://www.keypedia.com/companies/neotract-inc/7f7412d9-e532-4cda-84ea-7e32fd6cdd8d

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