# Siebert LLC, Coeur D Alene, ID – FDA Inspections

Source: https://www.keypedia.com/companies/siebert-llc/948f775b-978c-49ef-ac3a-ef9b7a367516

> Inspection records and compliance data for Siebert LLC in Coeur D Alene, Idaho. 6 FDA inspections on record (1 OAI), last inspected March 07, 2023.

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## Details

- Name: Siebert LLC
- FEI Number: 3006700324
- Address Line 1: 515 N 4th St # 3
- City: Coeur D Alene
- State: Idaho
- Zip Code: 83814
- Country Name: United States
- Address: 515 N 4th St # 3, Coeur D Alene, Idaho 83814, United States
- Country: United States

## Related Documents

- FDA Inspection 1200671 - Siebert LLC - 2023-03-07 — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2023
- FDA Inspection 1046167 - Siebert LLC - 2018-01-02 — classification: No Action Indicated (NAI), source: FDA, date: January 2, 2018
- FDA Inspection 914706 - Siebert LLC - 2015-01-29 — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2015
- FDA Inspection 914706 - Siebert LLC - 2015-01-29 — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2015
- [FDA Inspection 862758 - Siebert LLC - 2014-01-24](https://www.keypedia.com/records/fda_inspections/siebert-llc/ca78e751-bd63-483f-945a-9b5d5f25c398) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 24, 2014
- FDA Inspection 862758 - Siebert LLC - 2014-01-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 24, 2014
- FDA Inspection 824661 - Siebert LLC - 2013-04-23 — classification: Official Action Indicated (OAI), source: FDA, date: April 23, 2013
- [FDA Inspection 824661 - Siebert LLC - 2013-04-23](https://www.keypedia.com/records/fda_inspections/siebert-llc/65a8f670-2364-4d14-bd84-588b4b5b80b5) — classification: Official Action Indicated (OAI), source: FDA, date: April 23, 2013
- [FDA Inspection 777059 - Siebert LLC - 2012-04-06](https://www.keypedia.com/records/fda_inspections/siebert-llc/8570741d-256e-4f07-b830-803e74a72224) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 6, 2012

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