# Propper Mfg Co Inc – FDA Inspection, Oct 3, 2012

Source: https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/d2675e0f-eeed-436a-8903-377f96d6b758
Source feed: FDA_Inspections

> FDA inspection 802483 of Propper Mfg Co Inc, October 03, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 802483
- Company Name: Propper Mfg Co Inc
- Inspection Date: 2012-10-03
- 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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Company: https://www.keypedia.com/companies/propper-mfg-co-inc/534e89f5-bfae-43a7-b01c-9fe8d2fb5710

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