# FDA Inspection 1051492 - OR Specific, Inc. - March 20, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/or-specific-inc/5b686f31-5ad5-49e3-a7bb-634401b6badb
Source feed: FDA_Inspections

> FDA Inspection 1051492 for OR Specific, Inc. on March 20, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1051492
- Company Name: OR Specific, Inc.
- Inspection Date: 2018-03-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1051492 - 2018-03-20](https://www.globalkeysolutions.net/records/fda_inspections/or-specific-inc/614440fe-3244-4f1f-8593-b2b163db6115)
- [FDA Inspection 909492 - 2015-01-08](https://www.globalkeysolutions.net/records/fda_inspections/or-specific-inc/bf732ce3-b1dc-406c-8e46-9db4143a575c)
- [FDA Inspection 909492 - 2015-01-08](https://www.globalkeysolutions.net/records/fda_inspections/or-specific-inc/7e0734a0-0aaa-4176-b7a7-0491e9cdd7d3)

Company: https://www.globalkeysolutions.net/companies/or-specific-inc/83e040cf-dcae-479c-a3e7-0b816b5b15aa

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