# Reproductive Gynecology Laboratories, Akron, OH – FDA Inspections

Source: https://www.keypedia.com/companies/reproductive-gynecology-laboratories/3c4c1a9c-e596-40f9-95e1-cc6021f60622

> Inspection records and compliance data for Reproductive Gynecology Laboratories in Akron, Ohio. 7 FDA inspections on record, last inspected April 07, 2026.

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## Details

- Name: Reproductive Gynecology Laboratories
- FEI Number: 3003928276
- Address Line 1: 95 Arch St Ste 250
- City: Akron
- State: Ohio
- Zip Code: 44304
- Country Name: United States
- Address: 95 Arch St Ste 250, Akron, Ohio 44304, United States
- Country: United States

## Related Documents

- FDA Inspection 1312310 - Reproductive Gynecology Laboratories - 2026-04-07 — classification: No Action Indicated (NAI), source: FDA, date: April 7, 2026
- FDA Inspection 1194799 - Reproductive Gynecology Laboratories - 2023-01-10 — classification: No Action Indicated (NAI), source: FDA, date: January 10, 2023
- FDA Inspection 1194799 - Reproductive Gynecology Laboratories - 2023-01-10 — classification: No Action Indicated (NAI), source: FDA, date: January 10, 2023
- FDA Inspection 1194799 - Reproductive Gynecology Laboratories - 2023-01-10 — classification: No Action Indicated (NAI), source: FDA, date: January 10, 2023
- FDA Inspection 1110089 - Reproductive Gynecology Laboratories - 2019-11-07 — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2019
- FDA Inspection 1110089 - Reproductive Gynecology Laboratories - 2019-11-07 — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2019
- FDA Inspection 1032534 - Reproductive Gynecology Laboratories - 2017-11-28 — classification: No Action Indicated (NAI), source: FDA, date: November 28, 2017
- FDA Inspection 1032534 - Reproductive Gynecology Laboratories - 2017-11-28 — classification: No Action Indicated (NAI), source: FDA, date: November 28, 2017
- FDA Inspection 903327 - Reproductive Gynecology Laboratories - 2014-11-13 — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2014
- [FDA Inspection 813223 - Reproductive Gynecology Laboratories - 2013-01-15](https://www.keypedia.com/records/fda_inspections/reproductive-gynecology-laboratories/570f29e4-8fe0-4e78-8454-1e325a7ee1e7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 15, 2013

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