# Imperial Drug And Spice Company, West New York, NJ – FDA Inspections

Source: https://www.keypedia.com/companies/imperial-drug-and-spice-company/a893fd20-e5a4-4dbf-9493-022cc2dabfe5

> Inspection records and compliance data for Imperial Drug And Spice Company in West New York, New Jersey. 4 FDA inspections on record, last inspected September 13, 2022.

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## Details

- Name: Imperial Drug And Spice Company
- FEI Number: 3003089429
- Address Line 1: 5620 Kennedy Blvd W
- City: West New York
- State: New Jersey
- Zip Code: 07093
- Country Name: United States
- Address: 5620 Kennedy Blvd W, West New York, New Jersey 07093, United States
- Country: United States

## Related Documents

- FDA Inspection 1181017 - Imperial Drug And Spice Company - 2022-09-13 — classification: No Action Indicated (NAI), source: FDA, date: September 13, 2022
- FDA Inspection 1181017 - Imperial Drug And Spice Company - 2022-09-13 — classification: No Action Indicated (NAI), source: FDA, date: September 13, 2022
- FDA Inspection 993032 - Imperial Drug And Spice Company - 2016-10-26 — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2016
- [FDA Inspection 993032 - Imperial Drug And Spice Company - 2016-10-26](https://www.keypedia.com/records/fda_inspections/imperial-drug-and-spice-company/bdd068b2-3cc8-4726-85ea-a38332027d33) — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2016
- [FDA Inspection 779524 - Imperial Drug And Spice Company - 2012-04-26](https://www.keypedia.com/records/fda_inspections/imperial-drug-and-spice-company/e343631c-5e03-4d09-9745-64a9430ba0f2) — classification: No Action Indicated (NAI), source: FDA, date: April 26, 2012
- FDA Inspection 779524 - Imperial Drug And Spice Company - 2012-04-26 — classification: No Action Indicated (NAI), source: FDA, date: April 26, 2012
- [FDA Inspection 677959 - Imperial Drug And Spice Company - 2010-08-27](https://www.keypedia.com/records/fda_inspections/imperial-drug-and-spice-company/f8458bf9-2db5-4dd1-9650-c17075b55355) — classification: No Action Indicated (NAI), source: FDA, date: August 27, 2010

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