# Intercos America, Inc., Congers, NY – FDA Inspections

Source: https://www.keypedia.com/companies/intercos-america-inc/bae06734-84c6-406e-bee8-c0f0c45d9850

> Inspection records and compliance data for Intercos America, Inc. in Congers, New York. 6 FDA inspections on record, 1 Form 483, last inspected October 09, 2024.

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## Details

- Name: Intercos America, Inc.
- FEI Number: 3003361127
- Address Line 1: 200 N Route 303
- City: Congers
- State: New York
- Zip Code: 10920
- Country Name: United States
- Address: 200 N Route 303, Congers, New York 10920, United States
- Country: United States

## Related Documents

- [483 - Intercos America, Inc. - 2024-10-09](https://www.keypedia.com/records/483/intercos-america-inc/df857bb7-7bc3-4cf6-b9c2-3007689027f6) — source: FDA, date: October 9, 2024
- [FDA Inspection 1251393 - Intercos America, Inc. - 2024-10-09](https://www.keypedia.com/records/fda_inspections/intercos-america-inc/3e29e360-e155-4544-9e7f-2465a8f797a9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 9, 2024
- FDA Inspection 1209614 - Intercos America, Inc. - 2023-06-20 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2023
- [FDA Inspection 949580 - Intercos America, Inc. - 2015-11-24](https://www.keypedia.com/records/fda_inspections/intercos-america-inc/6094d300-8e08-4c9a-919e-9fba2144d3c3) — classification: No Action Indicated (NAI), source: FDA, date: November 24, 2015
- FDA Inspection 761254 - Intercos America, Inc. - 2011-12-28 — classification: No Action Indicated (NAI), source: FDA, date: December 28, 2011
- FDA Inspection 761254 - Intercos America, Inc. - 2011-12-28 — classification: No Action Indicated (NAI), source: FDA, date: December 28, 2011
- FDA Inspection 723418 - Intercos America, Inc. - 2011-05-04 — classification: No Action Indicated (NAI), source: FDA, date: May 4, 2011
- [FDA Inspection 652199 - Intercos America, Inc. - 2010-03-16](https://www.keypedia.com/records/fda_inspections/intercos-america-inc/8e1721c1-2866-4ad9-870a-accbe25e870f) — classification: No Action Indicated (NAI), source: FDA, date: March 16, 2010

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