# Pentax of America Inc – FDA Inspection, Mar 17, 2011

Source: https://www.keypedia.com/records/fda_inspections/pentax-of-america-inc/393821c2-8999-4d3c-a5c4-d57d9a9c5ea1
Source feed: FDA_Inspections

> FDA inspection 718354 of Pentax of America Inc, March 17, 2011. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 718354
- Company Name: Pentax of America Inc
- Inspection Date: 2011-03-17
- 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: 3

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- [FDA Inspection 921077 - 2015-04-02](https://www.keypedia.com/records/fda_inspections/pentax-of-america-inc/ea6db0bc-d56f-48a2-b2c8-67eb44596f7f)
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Company: https://www.keypedia.com/companies/pentax-of-america-inc/4a00a7fe-b951-46eb-8a88-2842b89a05ad

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