# Pinook USA, LLC – FDA Inspection, Mar 1, 2013

Source: https://www.keypedia.com/records/fda_inspections/pinook-usa-llc/99ca73eb-4cf1-407e-9171-36908cfaa412
Source feed: FDA_Inspections

> FDA inspection 821133 of Pinook USA, LLC, March 01, 2013. Classification: Official Action Indicated (OAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 821133
- Company Name: Pinook USA, LLC
- Inspection Date: 2013-03-01
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 927022 - 2015-05-13](https://www.keypedia.com/records/fda_inspections/pinook-usa-llc/9719bb64-3747-4b4d-8e66-633335c52cb7)
- [FDA Inspection 904825 - 2014-12-02](https://www.keypedia.com/records/fda_inspections/pinook-usa-llc/ff63f8b7-1d74-447c-bb1a-d6b7d343714c)
- [FDA Inspection 769446 - 2012-02-24](https://www.keypedia.com/records/fda_inspections/pinook-usa-llc/e514038e-cceb-459f-80ee-1469741d2900)

Company: https://www.keypedia.com/companies/pinook-usa-llc/49affed3-010f-4eee-9b84-2e376ee9dd64

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