# Brill Inc - Inspection Records

Source: https://www.globalkeysolutions.net/companies/brill-inc/68ad55d8-9e53-4fd1-b1a0-405923d69299

> Inspection records and compliance data for Brill Inc in Bonner Springs, Kansas. Access full analysis and detailed observations.

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## Details

- Name: Brill Inc
- FEI Number: 1927972
- City: Bonner Springs
- State: Kansas
- Country Name: United States
- Address Line 1: 2410 Scheidt Ln
- Zip Code: 66012

## Related Documents

- [FDA Inspection 834205 - Brill Inc - 2013-05-23](https://www.globalkeysolutions.net/records/fda_inspections/brill-inc/82f6301e-03de-4d78-bbf9-c8f2c61f53d7) — classification: No Action Indicated (NAI), source: FDA, date: May 23, 2013
- [FDA Inspection 724523 - Brill Inc - 2011-05-13](https://www.globalkeysolutions.net/records/fda_inspections/brill-inc/9bb58025-c3ff-449c-8a5e-878a6fecaf63) — classification: No Action Indicated (NAI), source: FDA, date: May 13, 2011
- [FDA Inspection 724523 - Brill Inc - 2011-05-13](https://www.globalkeysolutions.net/records/fda_inspections/brill-inc/6d0a8810-f078-4e1d-b50b-bc4f597f94a4) — classification: No Action Indicated (NAI), source: FDA, date: May 13, 2011
- [FDA Inspection 654431 - Brill Inc - 2010-03-18](https://www.globalkeysolutions.net/records/fda_inspections/brill-inc/06377a0f-de00-4a94-ac46-ec9ef699e3b1) — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2010
- [FDA Inspection 619857 - Brill Inc - 2009-10-13](https://www.globalkeysolutions.net/records/fda_inspections/brill-inc/7695d739-dd4d-4297-b728-9bd85071694e) — classification: No Action Indicated (NAI), source: FDA, date: October 13, 2009
- [FDA Inspection 619857 - Brill Inc - 2009-10-13](https://www.globalkeysolutions.net/records/fda_inspections/brill-inc/654580ac-c2f9-4ce1-82a4-ff459b2cbcbd) — classification: No Action Indicated (NAI), source: FDA, date: October 13, 2009
- [FDA Inspection 619857 - Brill Inc - 2009-10-13](https://www.globalkeysolutions.net/records/fda_inspections/brill-inc/feb6d93e-f7a8-41e8-8aa6-572e9fb86110) — classification: No Action Indicated (NAI), source: FDA, date: October 13, 2009

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