# FDA 483 - Perryman Company - October 10, 2019

Source: https://www.globalkeysolutions.net/records/483/perryman-company/7fa5c3c7-235f-4b36-b9aa-f7a8fff541b0

> FDA 483 for Perryman Company on October 10, 2019. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Perryman Company
- Inspection Date: 2019-10-10
- Product Type: device
- Office Name: Philadelphia District Office
- Summary: Perryman Company, a manufacturer of implantable medical devices in Houston, PA, was cited for two observations during an FDA inspection. The firm failed to adequately review and investigate customer rejection reports as complaints, and their procedures for corrective and preventive actions were not adequately established. These findings indicate deficiencies in the company's quality system regarding complaint handling and CAPA processes.

## Related Officers

- [issuing_officer](https://www.globalkeysolutions.net/people/dennis-r-hock/f13e2db1-b808-466d-a974-e5af2d5dfdb0)

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

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