# John Mantia & Sons Co., Inc. - Inspection Records

Source: https://www.keypedia.com/companies/john-mantia-sons-co-inc/e5e9fadd-4495-4024-8220-8f616101e646

> Inspection records and compliance data for John Mantia & Sons Co., Inc. in Boston, Massachusetts. Access full analysis and detailed observations.

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## Details

- Name: John Mantia & Sons Co., Inc.
- FEI Number: 1210035
- City: Boston
- State: Massachusetts
- Country Name: United States
- Address Line 1: 32-34 Fish Pier St W
- Zip Code: 02210

## Related Documents

- [FDA Inspection 1196593 - John Mantia & Sons Co., Inc. - 2023-01-31](https://www.keypedia.com/records/fda_inspections/john-mantia-sons-co-inc/0f69c015-37aa-478c-afd1-093536bde0bb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 31, 2023
- [FDA Inspection 1113318 - John Mantia & Sons Co., Inc. - 2019-12-19](https://www.keypedia.com/records/fda_inspections/john-mantia-sons-co-inc/3c6c74a0-3f3a-4bbe-8552-6449109c6a7d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 19, 2019
- [FDA Inspection 1113318 - John Mantia & Sons Co., Inc. - 2019-12-19](https://www.keypedia.com/records/fda_inspections/john-mantia-sons-co-inc/e5d221be-710f-49e7-ae50-ba8bb422830a) — classification: No Action Indicated (NAI), source: FDA, date: December 19, 2019
- [FDA Inspection 904675 - John Mantia & Sons Co., Inc. - 2014-11-21](https://www.keypedia.com/records/fda_inspections/john-mantia-sons-co-inc/80b727d7-0a63-41a9-8666-bcafa846c342) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 21, 2014
- [FDA Inspection 726111 - John Mantia & Sons Co., Inc. - 2011-05-23](https://www.keypedia.com/records/fda_inspections/john-mantia-sons-co-inc/8db0f69a-2628-40c2-a316-238dc9b744c5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 23, 2011
- [FDA Inspection 590128 - John Mantia & Sons Co., Inc. - 2009-06-18](https://www.keypedia.com/records/fda_inspections/john-mantia-sons-co-inc/78b0e747-9c80-4a2e-b45a-c10b9538a00a) — classification: No Action Indicated (NAI), source: FDA, date: June 18, 2009

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