# E.W. Grobbel Sons Inc dbas Grobbel, Sy Ginsberg, Topor s and Ba Tampte - Inspection Records

Source: https://www.keypedia.com/companies/ew-grobbel-sons-inc-dbas-grobbel-sy-ginsberg-topor-s-and-ba-tampte/a8d06c3f-d13c-437f-a4dc-c61301b5b587

> Inspection records and compliance data for E.W. Grobbel Sons Inc dbas Grobbel, Sy Ginsberg, Topor s and Ba Tampte in Taylor, Michigan. Access full analysis and detailed observations.

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## Details

- Name: E.W. Grobbel Sons Inc dbas Grobbel, Sy Ginsberg, Topor s and Ba Tampte
- FEI Number: 1816478
- City: Taylor
- State: Michigan
- Country Name: United States
- Address Line 1: 7640 Holland Rd
- Zip Code: 48180

## Related Documents

- [FDA Inspection 860798 - E.W. Grobbel Sons Inc dbas Grobbel, Sy Ginsberg, Topor s and Ba Tampte - 2013-12-10](https://www.keypedia.com/records/fda_inspections/ew-grobbel-sons-inc-dbas-grobbel-sy-ginsberg-topor-s-and-ba-tampte/5c0f9c0c-21e5-4e26-96cf-c89fab540637) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 10, 2013
- [FDA Inspection 781299 - E.W. Grobbel Sons Inc dbas Grobbel, Sy Ginsberg, Topor s and Ba Tampte - 2012-05-14](https://www.keypedia.com/records/fda_inspections/ew-grobbel-sons-inc-dbas-grobbel-sy-ginsberg-topor-s-and-ba-tampte/029433f9-251b-4924-8ea3-93be3de9a3b5) — classification: No Action Indicated (NAI), source: FDA, date: May 14, 2012
- [FDA Inspection 698500 - E.W. Grobbel Sons Inc dbas Grobbel, Sy Ginsberg, Topor s and Ba Tampte - 2010-11-22](https://www.keypedia.com/records/fda_inspections/ew-grobbel-sons-inc-dbas-grobbel-sy-ginsberg-topor-s-and-ba-tampte/1e94ee5e-1bee-40e5-918f-2732416668ea) — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2010
- [FDA Inspection 629616 - E.W. Grobbel Sons Inc dbas Grobbel, Sy Ginsberg, Topor s and Ba Tampte - 2009-11-10](https://www.keypedia.com/records/fda_inspections/ew-grobbel-sons-inc-dbas-grobbel-sy-ginsberg-topor-s-and-ba-tampte/5df98fb7-fe70-4fe7-aa73-5467e82561a7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 10, 2009

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