# Propper Mfg Co Inc, Long Island City, NY – FDA Inspections

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. 6 FDA inspections on record, 1 Form 483, last inspected June 13, 2024.

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## Details

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

## Related Documents

- FDA Inspection 1242777 - Propper Mfg Co Inc - 2024-06-13 — 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 — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2021
- FDA Inspection 1152179 - Propper Mfg Co Inc - 2021-09-14 — 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/bcef571b-c9dd-4072-86f4-fc70d970192f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 21, 2017
- FDA Inspection 1035639 - Propper Mfg Co Inc - 2017-12-21 — 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/d2675e0f-eeed-436a-8903-377f96d6b758) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 3, 2012
- FDA Inspection 802483 - Propper Mfg Co Inc - 2012-10-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 3, 2012
- FDA Inspection 696082 - Propper Mfg Co Inc - 2010-10-27 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 27, 2010

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