# Mississippi Reproductive Medicine, LLC, Flowood, MS – FDA Inspections

Source: https://www.keypedia.com/companies/mississippi-reproductive-medicine-llc/dfa05025-dccb-48b4-bc22-4c4ca3764e54

> Inspection records and compliance data for Mississippi Reproductive Medicine, LLC in Flowood, Mississippi. 6 FDA inspections on record, last inspected January 31, 2024.

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## Details

- Name: Mississippi Reproductive Medicine, LLC
- FEI Number: 3008816513
- Address Line 1: 2500 Lakeland Dr
- City: Flowood
- State: Mississippi
- Zip Code: 39232
- Country Name: United States
- Address: 2500 Lakeland Dr, Flowood, Mississippi 39232, United States
- Country: United States

## Related Documents

- FDA Inspection 1229964 - Mississippi Reproductive Medicine, LLC - 2024-01-31 — classification: No Action Indicated (NAI), source: FDA, date: January 31, 2024
- FDA Inspection 1229964 - Mississippi Reproductive Medicine, LLC - 2024-01-31 — classification: No Action Indicated (NAI), source: FDA, date: January 31, 2024
- FDA Inspection 1177997 - Mississippi Reproductive Medicine, LLC - 2022-07-27 — classification: No Action Indicated (NAI), source: FDA, date: July 27, 2022
- FDA Inspection 1177997 - Mississippi Reproductive Medicine, LLC - 2022-07-27 — classification: No Action Indicated (NAI), source: FDA, date: July 27, 2022
- FDA Inspection 1177997 - Mississippi Reproductive Medicine, LLC - 2022-07-27 — classification: No Action Indicated (NAI), source: FDA, date: July 27, 2022
- FDA Inspection 1066807 - Mississippi Reproductive Medicine, LLC - 2018-09-07 — classification: No Action Indicated (NAI), source: FDA, date: September 7, 2018
- FDA Inspection 982415 - Mississippi Reproductive Medicine, LLC - 2016-08-17 — classification: No Action Indicated (NAI), source: FDA, date: August 17, 2016
- FDA Inspection 876077 - Mississippi Reproductive Medicine, LLC - 2014-04-24 — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2014
- FDA Inspection 742223 - Mississippi Reproductive Medicine, LLC - 2011-08-18 — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2011

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