# Sterling Wisconsin, LLC - Inspection Records

Source: https://www.keypedia.com/companies/sterling-wisconsin-llc/1bef3270-1910-4a5c-bef6-4d3cb443a44d

> Inspection records and compliance data for Sterling Wisconsin, LLC in Germantown, Wisconsin. Access full analysis and detailed observations.

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## Details

- Name: Sterling Wisconsin, LLC
- FEI Number: 3004485164
- City: Germantown
- State: Wisconsin
- Country Name: United States
- Address Line 1: W132n10550 Grant Dr
- Zip Code: 53022
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1231382 - Sterling Wisconsin, LLC - 2024-03-12](https://www.keypedia.com/records/fda_inspections/sterling-wisconsin-llc/ad691ad4-6ae4-47ed-bba1-fc52466760a9) — classification: No Action Indicated (NAI), source: FDA, date: March 12, 2024
- [FDA Inspection 978639 - Sterling Wisconsin, LLC - 2016-06-24](https://www.keypedia.com/records/fda_inspections/sterling-wisconsin-llc/b874c823-b37d-4bef-951b-a34d23655ba2) — classification: No Action Indicated (NAI), source: FDA, date: June 24, 2016
- [FDA Inspection 849051 - Sterling Wisconsin, LLC - 2013-09-18](https://www.keypedia.com/records/fda_inspections/sterling-wisconsin-llc/58e9687a-18f7-4365-be4c-77bb8f582cf2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 18, 2013
- [FDA Inspection 759276 - Sterling Wisconsin, LLC - 2011-12-16](https://www.keypedia.com/records/fda_inspections/sterling-wisconsin-llc/cec9e37e-f482-4c12-8857-29b403da1d94) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 16, 2011
- [FDA Inspection 599787 - Sterling Wisconsin, LLC - 2009-08-04](https://www.keypedia.com/records/fda_inspections/sterling-wisconsin-llc/2301295d-309c-4dab-bbe2-449f10c02759) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 4, 2009
- [FDA Inspection 599789 - Sterling Wisconsin, LLC - 2009-08-04](https://www.keypedia.com/records/fda_inspections/sterling-wisconsin-llc/6a93f8e2-6fc1-465b-881b-df49da040d71) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 4, 2009

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