# FDA Inspection 1242777 - Propper Mfg Co Inc - June 13, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/propper-mfg-co-inc/ff0e7ad1-b200-4591-8c60-c446990785b1/
Source feed: FDA_Inspections

> FDA Inspection 1242777 for Propper Mfg Co Inc on June 13, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1242777
- Company Name: Propper Mfg Co Inc
- Inspection Date: 2024-06-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1242777 - 2024-06-13](https://www.globalkeysolutions.net/api/records/fda_inspections/propper-mfg-co-inc/a6fc289b-0a98-469d-af7d-02da820b61fb/)
- [FDA Inspection 1152179 - 2021-09-14](https://www.globalkeysolutions.net/api/records/fda_inspections/propper-mfg-co-inc/5833c75b-5284-4abd-84c8-46f14b315dfe/)
- [FDA Inspection 1152179 - 2021-09-14](https://www.globalkeysolutions.net/api/records/fda_inspections/propper-mfg-co-inc/4fe04b05-c73a-4e58-89e9-936aa8238111/)
- [FDA Inspection 1035639 - 2017-12-21](https://www.globalkeysolutions.net/api/records/fda_inspections/propper-mfg-co-inc/2b5a9ab2-d97c-4e81-8dfb-f849364ba729/)
- [FDA Inspection 1035639 - 2017-12-21](https://www.globalkeysolutions.net/api/records/fda_inspections/propper-mfg-co-inc/bcef571b-c9dd-4072-86f4-fc70d970192f/)

Company: https://www.globalkeysolutions.net/companies/propper-mfg-co-inc/534e89f5-bfae-43a7-b01c-9fe8d2fb5710

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