# Eagle Products & Services, LLC, South Plainfield, NJ – FDA Inspections

Source: https://www.keypedia.com/companies/eagle-products-services-llc/87303104-bb3b-4489-96c1-80c50dd0e3b7

> Inspection records and compliance data for Eagle Products & Services, LLC in South Plainfield, New Jersey. 6 FDA inspections on record, 1 Form 483, last inspected June 13, 2018.

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## Details

- Name: Eagle Products & Services, LLC
- FEI Number: 3009318559
- Address Line 1: 2101 Parker Ave
- City: South Plainfield
- State: New Jersey
- Zip Code: 07080
- Country Name: United States
- Address: 2101 Parker Ave, South Plainfield, New Jersey 07080, United States
- Country: United States

## Related Documents

- [FDA Inspection 1055534 - Eagle Products & Services, LLC - 2018-06-13](https://www.keypedia.com/records/fda_inspections/eagle-products-services-llc/d26ff412-b3d0-4b18-b51c-c1ae7cb0a514) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 13, 2018
- [FDA Inspection 939129 - Eagle Products & Services, LLC - 2015-07-27](https://www.keypedia.com/records/fda_inspections/eagle-products-services-llc/9491b200-5772-4ce8-a055-629f791bf734) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 27, 2015
- FDA Inspection 761657 - Eagle Products & Services, LLC - 2012-01-04 — classification: No Action Indicated (NAI), source: FDA, date: January 4, 2012
- [FDA Inspection 709705 - Eagle Products & Services, LLC - 2011-02-18](https://www.keypedia.com/records/fda_inspections/eagle-products-services-llc/cf4bfa02-3442-46a7-8b4c-d7e971f5d42c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 18, 2011
- [FDA Inspection 616825 - Eagle Products & Services, LLC - 2009-10-01](https://www.keypedia.com/records/fda_inspections/eagle-products-services-llc/6d8fc84c-acde-4e41-9115-172e52217eb0) — classification: No Action Indicated (NAI), source: FDA, date: October 1, 2009
- FDA Inspection 549009 - Eagle Products & Services, LLC - 2008-12-02 — classification: No Action Indicated (NAI), source: FDA, date: December 2, 2008

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