# Propper Mfg Co Inc – FDA Inspection, Dec 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/bcef571b-c9dd-4072-86f4-fc70d970192f
Source feed: FDA_Inspections

> FDA inspection 1035639 of Propper Mfg Co Inc, December 21, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1035639
- Company Name: Propper Mfg Co Inc
- Inspection Date: 2017-12-21
- 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 1152179 - 2021-09-14
- [FDA Inspection 918916 - 2015-03-18](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/a2394f61-afae-4d32-963b-b69dcb6cb9c7)
- [FDA Inspection 802483 - 2012-10-03](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/d2675e0f-eeed-436a-8903-377f96d6b758)
- [FDA Inspection 696082 - 2010-10-27](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/e854a45c-4574-466b-b52d-ae73f4349e9a)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/andrew-j-garufi/567f6aaa-f6f2-45a3-9a58-80b33f3ad021)

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