# Pemco Inc – FDA Inspection, Oct 25, 2016

Source: https://www.keypedia.com/records/fda_inspections/pemco-inc/a3a23542-df33-48cb-be69-ac3a18b3a873
Source feed: FDA_Inspections

> FDA inspection 990485 of Pemco Inc, October 25, 2016. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803, 806 and 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 990485
- Company Name: Pemco Inc
- Inspection Date: 2016-10-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

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- FDA Inspection 1158882 - 2021-12-16
- FDA Inspection 809014 - 2012-12-05
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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/benjamin-j-dastoli/688c2ad7-f7ac-47eb-8ca2-4efcd221f636)

Company: https://www.keypedia.com/companies/pemco-inc/83baa591-16b5-4a52-be13-f961caee69e8

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