# Penlon Limited – FDA Inspection, Sep 13, 2018

Source: https://www.keypedia.com/records/fda_inspections/penlon-limited/c3677278-4836-41eb-97ab-b6ad74b63f0c
Source feed: FDA_Inspections

> FDA inspection 1065790 of Penlon Limited, September 13, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1065790
- Company Name: Penlon Limited
- Inspection Date: 2018-09-13
- 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

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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/stephen-c-smith/426649fa-0e5b-4b35-ba41-636512a06a48)

Company: https://www.keypedia.com/companies/penlon-limited/14be701b-30b1-46c4-a66f-15a96925af9f

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