# Propper Mfg Co Inc - Inspection Records

Source: https://www.keypedia.com/companies/propper-mfg-co-inc/534e89f5-bfae-43a7-b01c-9fe8d2fb5710

> Inspection records and compliance data for Propper Mfg Co Inc in Long Island City, New York. Access full analysis and detailed observations.

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## Details

- Name: Propper Mfg Co Inc
- FEI Number: 2410251
- City: Long Island City
- State: New York
- Country Name: United States
- Address Line 1: 3604 Skillman Ave
- Zip Code: 11101

## Related Documents

- [FDA Inspection 1242777 - Propper Mfg Co Inc - 2024-06-13](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/a6fc289b-0a98-469d-af7d-02da820b61fb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 13, 2024
- [FDA Inspection 1242777 - Propper Mfg Co Inc - 2024-06-13](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/ff0e7ad1-b200-4591-8c60-c446990785b1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 13, 2024
- [FDA Inspection 1152179 - Propper Mfg Co Inc - 2021-09-14](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/4fe04b05-c73a-4e58-89e9-936aa8238111) — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2021
- [FDA Inspection 1152179 - Propper Mfg Co Inc - 2021-09-14](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/5833c75b-5284-4abd-84c8-46f14b315dfe) — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2021
- [FDA Inspection 1035639 - Propper Mfg Co Inc - 2017-12-21](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/2b5a9ab2-d97c-4e81-8dfb-f849364ba729) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 21, 2017
- [FDA Inspection 1035639 - Propper Mfg Co Inc - 2017-12-21](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/bcef571b-c9dd-4072-86f4-fc70d970192f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 21, 2017
- [FDA Inspection 918916 - Propper Mfg Co Inc - 2015-03-18](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/a2394f61-afae-4d32-963b-b69dcb6cb9c7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2015
- [FDA Inspection 802483 - Propper Mfg Co Inc - 2012-10-03](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/0f83a175-6cad-4063-a0c7-fe7d6663ef78) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 3, 2012
- [FDA Inspection 802483 - Propper Mfg Co Inc - 2012-10-03](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/d2675e0f-eeed-436a-8903-377f96d6b758) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 3, 2012
- [FDA Inspection 696082 - Propper Mfg Co Inc - 2010-10-27](https://www.keypedia.com/records/fda_inspections/propper-mfg-co-inc/04094c7f-a34e-430a-9b38-c1b2a559e190) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 27, 2010

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