# RMA Long Island IVF, Melville, NY – FDA Inspections

Source: https://www.keypedia.com/companies/rma-long-island-ivf/cd54c3fa-c54b-41c1-a844-8eafdb85b4f3

> Inspection records and compliance data for RMA Long Island IVF in Melville, New York. 8 FDA inspections on record, last inspected February 09, 2024.

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## Details

- Name: RMA Long Island IVF
- FEI Number: 3007067646
- Address Line 1: 8 Corporate Center Dr Ste 101
- City: Melville
- State: New York
- Zip Code: 11747
- Country Name: United States
- Address: 8 Corporate Center Dr Ste 101, Melville, New York 11747, United States
- Country: United States

## Related Documents

- [483 - RMA Long Island IVF - 2024-02-09](https://www.keypedia.com/records/483/rma-long-island-ivf/cd0700b1-a825-46e0-bd12-ad43b5937daa) — source: FDA, date: February 9, 2024
- [FDA Inspection 1229041 - RMA Long Island IVF - 2024-02-09](https://www.keypedia.com/records/fda_inspections/rma-long-island-ivf/d3a572d3-1795-41a8-840a-52327db22793) — classification: No Action Indicated (NAI), source: FDA, date: February 9, 2024
- FDA Inspection 1229041 - RMA Long Island IVF - 2024-02-09 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 9, 2024
- [483 - RMA Long Island IVF - 2022-03-01](https://www.keypedia.com/records/483/rma-long-island-ivf/28eb2e2c-2d3c-4993-bb38-0b030aecf5e6) — source: FDA, date: March 1, 2022
- FDA Inspection 1163524 - RMA Long Island IVF - 2022-03-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 1, 2022
- FDA Inspection 1163524 - RMA Long Island IVF - 2022-03-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 1, 2022
- FDA Inspection 1163524 - RMA Long Island IVF - 2022-03-01 — classification: No Action Indicated (NAI), source: FDA, date: March 1, 2022
- FDA Inspection 1076523 - RMA Long Island IVF - 2018-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2018
- FDA Inspection 1076523 - RMA Long Island IVF - 2018-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2018
- FDA Inspection 994705 - RMA Long Island IVF - 2016-12-20 — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2016
- FDA Inspection 994705 - RMA Long Island IVF - 2016-12-20 — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2016
- FDA Inspection 900033 - RMA Long Island IVF - 2014-10-16 — classification: No Action Indicated (NAI), source: FDA, date: October 16, 2014

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