# Boston IVF, Inc. The Maine Center, S Portland, ME – FDA Inspections

Source: https://www.keypedia.com/companies/boston-ivf-inc-the-maine-center/60aa035b-226e-4ecd-94df-027528c6c3c2

> Inspection records and compliance data for Boston IVF, Inc. The Maine Center in S Portland, Maine. 6 FDA inspections on record, last inspected April 15, 2025.

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## Details

- Name: Boston IVF, Inc. The Maine Center
- FEI Number: 3008339013
- Address Line 1: 778 Main St
- City: S Portland
- State: Maine
- Zip Code: 04106
- Country Name: United States
- Address: 778 Main St, S Portland, Maine 04106, United States
- Country: United States

## Related Documents

- FDA Inspection 1267633 - Boston IVF, Inc. The Maine Center - 2025-04-15 — source: FDA, date: April 15, 2025
- FDA Inspection 1267633 - Boston IVF, Inc. The Maine Center - 2025-04-15 — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2025
- FDA Inspection 1198033 - Boston IVF, Inc. The Maine Center - 2023-02-17 — classification: No Action Indicated (NAI), source: FDA, date: February 17, 2023
- FDA Inspection 1198033 - Boston IVF, Inc. The Maine Center - 2023-02-17 — classification: No Action Indicated (NAI), source: FDA, date: February 17, 2023
- FDA Inspection 1198033 - Boston IVF, Inc. The Maine Center - 2023-02-17 — classification: No Action Indicated (NAI), source: FDA, date: February 17, 2023
- FDA Inspection 1102767 - Boston IVF, Inc. The Maine Center - 2019-08-01 — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2019
- FDA Inspection 1102767 - Boston IVF, Inc. The Maine Center - 2019-08-01 — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2019
- FDA Inspection 1015451 - Boston IVF, Inc. The Maine Center - 2017-06-01 — classification: No Action Indicated (NAI), source: FDA, date: June 1, 2017
- FDA Inspection 913317 - Boston IVF, Inc. The Maine Center - 2015-01-15 — classification: No Action Indicated (NAI), source: FDA, date: January 15, 2015
- FDA Inspection 815966 - Boston IVF, Inc. The Maine Center - 2013-01-24 — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2013

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