# FDA Inspection 1307166 - Perryman Company - March 10, 2026

Source: https://www.keypedia.com/records/fda_inspections/perryman-company/1728517d-3b78-4015-aedb-433f7fbaa9fa
Source feed: FDA_Inspections

> FDA inspection 1307166 of Perryman Company, March 10, 2026. Classification: Voluntary Action Indicated (VAI). 4 citations. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1307166
- Company Name: Perryman Company
- Inspection Date: 2026-03-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Philadelphia District Office
- Citation Count: 4

## Related Documents

- [FDA Inspection 1106963 - 2019-10-10](https://www.keypedia.com/records/fda_inspections/perryman-company/8efa677d-4e36-4947-84d8-112f9c581481)
- FDA Inspection 1005622 - 2017-02-09
- FDA Inspection 941493 - 2015-09-10

## Related Officers

- [Company Rep](https://www.keypedia.com/people/dennis-r-hock/f13e2db1-b808-466d-a974-e5af2d5dfdb0)

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

Office: https://www.keypedia.com/offices/philadelphia-district-office/c5ec7398-b3d5-4125-9793-fb7b972578d8