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

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

> FDA inspection 1106963 of Perryman Company, October 10, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1106963
- Company Name: Perryman Company
- Inspection Date: 2019-10-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1307166 - 2026-03-10](https://www.keypedia.com/records/fda_inspections/perryman-company/1728517d-3b78-4015-aedb-433f7fbaa9fa)
- FDA Inspection 1005622 - 2017-02-09
- FDA Inspection 941493 - 2015-09-10

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

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