# Burnham & Morrill Company - Inspection Records

Source: https://www.globalkeysolutions.net/companies/burnham-morrill-company/248368cf-f5e9-46e4-8402-1be11b6a5b62

> Inspection records and compliance data for Burnham & Morrill Company in Portland, Maine. Access full analysis and detailed observations.

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## Details

- Name: Burnham & Morrill Company
- FEI Number: 1210593
- City: Portland
- State: Maine
- Country Name: United States
- Address Line 1: 1 Beanpot Cir
- Zip Code: 04103

## Related Documents

- [FDA Inspection 1053969 - Burnham & Morrill Company - 2018-04-20](https://www.globalkeysolutions.net/records/fda_inspections/burnham-morrill-company/8833bfb4-8190-4c6d-aee9-d6903ddf4add) — classification: No Action Indicated (NAI), source: FDA, date: April 20, 2018
- [FDA Inspection 936346 - Burnham & Morrill Company - 2015-07-09](https://www.globalkeysolutions.net/records/fda_inspections/burnham-morrill-company/b90915f8-b413-4840-8f7c-6519ece74632) — classification: No Action Indicated (NAI), source: FDA, date: July 9, 2015
- [FDA Inspection 791774 - Burnham & Morrill Company - 2012-07-18](https://www.globalkeysolutions.net/records/fda_inspections/burnham-morrill-company/e6eefea5-04e4-437c-930f-7aec117f911c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 18, 2012
- [FDA Inspection 722332 - Burnham & Morrill Company - 2011-04-29](https://www.globalkeysolutions.net/records/fda_inspections/burnham-morrill-company/7c21e8ef-d05a-4d19-817b-8c6532627659) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 29, 2011
- [FDA Inspection 658406 - Burnham & Morrill Company - 2010-04-21](https://www.globalkeysolutions.net/records/fda_inspections/burnham-morrill-company/f2ad7cb7-a4aa-4385-90ee-4779973a7962) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 21, 2010
- [FDA Inspection 613198 - Burnham & Morrill Company - 2009-09-03](https://www.globalkeysolutions.net/records/fda_inspections/burnham-morrill-company/7acf0d48-8919-4710-a38c-9c8b4be9ff35) — classification: No Action Indicated (NAI), source: FDA, date: September 3, 2009

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