# FDA Inspection 1106963 - Perryman Company - October 10, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/perryman-company/8efa677d-4e36-4947-84d8-112f9c581481
Source feed: FDA_Inspections

> FDA Inspection 1106963 for Perryman Company on October 10, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1106963
- Company Name: Perryman Company
- Inspection Date: 2019-10-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/perryman-company/0018ea83-8ef1-4d46-bb8d-aaa94e2e285c

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