# RMA Long Island IVF - Inspection Records

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. Access full analysis and detailed observations.

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## Details

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

## 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/a002b209-413e-463b-923c-a07071d2a390) — classification: Voluntary Action Indicated (VAI), 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
- [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](https://www.keypedia.com/records/fda_inspections/rma-long-island-ivf/b72efe13-42e1-42cd-9810-2c4687667497) — classification: No Action Indicated (NAI), source: FDA, date: March 1, 2022
- [FDA Inspection 1163524 - RMA Long Island IVF - 2022-03-01](https://www.keypedia.com/records/fda_inspections/rma-long-island-ivf/d684c246-3d74-4f0d-a5a8-51258fd527fb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 1, 2022
- [FDA Inspection 1163524 - RMA Long Island IVF - 2022-03-01](https://www.keypedia.com/records/fda_inspections/rma-long-island-ivf/ec5d5846-1dc9-4b46-a8fb-391bc3c7139d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 1, 2022
- [FDA Inspection 1076523 - RMA Long Island IVF - 2018-12-13](https://www.keypedia.com/records/fda_inspections/rma-long-island-ivf/e6502ecd-8238-45cf-96fc-2fbe2e4113f9) — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2018
- [FDA Inspection 1076523 - RMA Long Island IVF - 2018-12-13](https://www.keypedia.com/records/fda_inspections/rma-long-island-ivf/b7b610e3-033b-4a6c-aa96-4aa3ca7cd1e5) — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2018
- [FDA Inspection 994705 - RMA Long Island IVF - 2016-12-20](https://www.keypedia.com/records/fda_inspections/rma-long-island-ivf/231caad2-f044-4ad1-b857-7a7f2a1ae55f) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2016
- [FDA Inspection 994705 - RMA Long Island IVF - 2016-12-20](https://www.keypedia.com/records/fda_inspections/rma-long-island-ivf/0fadf0ab-7dfe-48ec-88db-7d098febfd87) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2016
- [FDA Inspection 900033 - RMA Long Island IVF - 2014-10-16](https://www.keypedia.com/records/fda_inspections/rma-long-island-ivf/c16bb37f-d32e-4d38-a2bb-5699b36a29d8) — classification: No Action Indicated (NAI), source: FDA, date: October 16, 2014

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