# Sumbaker GP, Memphis, TN – FDA Inspections

Source: https://www.keypedia.com/companies/sumbaker-gp/13e357c5-5065-4bba-960d-cc3e2d90512f

> Inspection records and compliance data for Sumbaker GP in Memphis, Tennessee. 7 FDA inspections on record, last inspected April 29, 2026.

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## Details

- Name: Sumbaker GP
- FEI Number: 3004109642
- Address Line 1: 5041 Summer Ave
- City: Memphis
- State: Tennessee
- Zip Code: 38122
- Country Name: United States
- Address: 5041 Summer Ave, Memphis, Tennessee 38122, United States
- Country: United States

## Related Documents

- FDA Inspection 1315530 - Sumbaker GP - 2026-04-29 — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2026
- [FDA Inspection 1315530 - Sumbaker GP - 2026-04-29](https://www.keypedia.com/records/fda_inspections/sumbaker-gp/8d3e4143-45dd-47c5-beac-0b43da52c4a5) — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2026
- FDA Inspection 1232729 - Sumbaker GP - 2024-03-07 — source: FDA, date: March 7, 2024
- [FDA Inspection 1108762 - Sumbaker GP - 2019-10-31](https://www.keypedia.com/records/fda_inspections/sumbaker-gp/d5000701-b688-46a7-be7c-270b6810bee0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 31, 2019
- FDA Inspection 997485 - Sumbaker GP - 2016-12-06 — classification: No Action Indicated (NAI), source: FDA, date: December 6, 2016
- [FDA Inspection 768507 - Sumbaker GP - 2012-02-15](https://www.keypedia.com/records/fda_inspections/sumbaker-gp/21fae09d-f7bc-4860-b177-dbda79c1429b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 15, 2012
- [FDA Inspection 715883 - Sumbaker GP - 2011-03-24](https://www.keypedia.com/records/fda_inspections/sumbaker-gp/49fedc2a-e2e7-415e-b984-54a16860c6ee) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 24, 2011
- FDA Inspection 715883 - Sumbaker GP - 2011-03-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 24, 2011
- FDA Inspection 575622 - Sumbaker GP - 2009-04-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 3, 2009

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