# FDA Inspection 1023316 - Frank Arko - August 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/frank-arko/9bc3c974-47de-4446-914c-648a9632c3ea
Source feed: FDA_Inspections

> FDA Inspection 1023316 for Frank Arko on August 14, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023316
- Company Name: Frank Arko
- Inspection Date: 2017-08-14
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/frank-arko/3953fac5-2e57-4216-8284-6d27cea96b98

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