FDA Inspection
Propper Mfg Co IncPropper Mfg Co Inc – FDA Inspection, Oct 3, 2012
Record Details
This FDA Inspection record concerns Propper Mfg Co Inc, with an inspection on October 3, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Propper Mfg Co Inc
- Inspection Date
- October 3, 2012
- Product Type
- Devices
View Company Profile
ID · d2675e0f-eeed-436a-8903-377f96d6b758
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 802483
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Complaints
- 21 CFR 820.100(b)Documentation
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Other FDA inspections of Propper Mfg Co Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| June 13, 2024 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| 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 27, 2010 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Propper Mfg Co Inc
- FDA Inspection 1242777 - 2024-06-13
- FDA Inspection 1152179 - 2021-09-14
- FDA Inspection 1035639 - 2017-12-21
- FDA Inspection 918916 - 2015-03-18
- FDA Inspection 696082 - 2010-10-27
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