FDA Inspection
Propper Mfg Co IncPropper Mfg Co Inc – FDA Inspection, Jun 13, 2024
Record Details
This FDA Inspection record concerns Propper Mfg Co Inc, with an inspection on June 13, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · ff0e7ad1-b200-4591-8c60-c446990785b1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1242777
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.70(g)Equipment Installation, Placement, Specified Requirements
- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Propper Mfg Co Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| September 14, 2021 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 21, 2017 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 18, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 3, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 27, 2010 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Propper Mfg Co Inc
- FDA Inspection 1152179 - 2021-09-14
- FDA Inspection 1035639 - 2017-12-21
- FDA Inspection 918916 - 2015-03-18
- FDA Inspection 802483 - 2012-10-03
- FDA Inspection 696082 - 2010-10-27
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