# Galbraith Laboratories Inc - Inspection Records

Source: https://www.keypedia.com/companies/galbraith-laboratories-inc/6a269a6c-2d54-487f-93d9-8939dc052c2d

> Inspection records and compliance data for Galbraith Laboratories Inc in Knoxville, Tennessee. Access full analysis and detailed observations.

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## Details

- Name: Galbraith Laboratories Inc
- FEI Number: 1000112629
- City: Knoxville
- State: Tennessee
- Country Name: United States
- Address Line 1: 2323 Sycamore Dr
- Zip Code: 37921
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1322240 - Galbraith Laboratories Inc - 2026-06-16](https://www.keypedia.com/records/fda_inspections/galbraith-laboratories-inc/4080e79f-f658-4d35-ae2f-7046ba3b9ea2) — source: FDA, date: June 16, 2026
- [483 - Galbraith Laboratories Inc - 2023-11-16](https://www.keypedia.com/records/483/galbraith-laboratories-inc/041a6eb6-c541-4c83-af78-47857aaa75c1) — source: FDA, date: November 16, 2023
- [FDA Inspection 1222900 - Galbraith Laboratories Inc - 2023-11-16](https://www.keypedia.com/records/fda_inspections/galbraith-laboratories-inc/4cadf4b4-0c80-4dd1-9c4f-9da73da15165) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 16, 2023
- [483 - Galbraith Laboratories Inc - 2022-03-02](https://www.keypedia.com/records/483/galbraith-laboratories-inc/67d2319b-7e82-4720-b800-0978b4a88632) — source: FDA, date: March 2, 2022
- [FDA Inspection 1163571 - Galbraith Laboratories Inc - 2022-03-02](https://www.keypedia.com/records/fda_inspections/galbraith-laboratories-inc/a135ac1d-f253-4053-9753-22f87960aefa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 2, 2022
- [FDA Inspection 993886 - Galbraith Laboratories Inc - 2016-12-01](https://www.keypedia.com/records/fda_inspections/galbraith-laboratories-inc/f6739a6e-073d-4a52-b558-401a88076de3) — classification: No Action Indicated (NAI), source: FDA, date: December 1, 2016
- [FDA Inspection 905657 - Galbraith Laboratories Inc - 2014-12-03](https://www.keypedia.com/records/fda_inspections/galbraith-laboratories-inc/93e2916a-3bd9-4af6-ae36-c75e5de3b8d4) — classification: No Action Indicated (NAI), source: FDA, date: December 3, 2014
- [FDA Inspection 867685 - Galbraith Laboratories Inc - 2014-02-11](https://www.keypedia.com/records/fda_inspections/galbraith-laboratories-inc/2f730bf0-53d6-4c82-b28e-9c8d6f085dd2) — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2014
- [FDA Inspection 867685 - Galbraith Laboratories Inc - 2014-02-11](https://www.keypedia.com/records/fda_inspections/galbraith-laboratories-inc/6bc680f2-5311-46ca-b6af-cb5a67d2017a) — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2014
- [FDA Inspection 714534 - Galbraith Laboratories Inc - 2011-03-09](https://www.keypedia.com/records/fda_inspections/galbraith-laboratories-inc/1e696414-e6c9-4691-ad9a-a65aabdb1a7c) — classification: No Action Indicated (NAI), source: FDA, date: March 9, 2011
- [FDA Inspection 681621 - Galbraith Laboratories Inc - 2010-09-07](https://www.keypedia.com/records/fda_inspections/galbraith-laboratories-inc/fcdb210d-adfd-453d-b530-4e2e6bb878c4) — classification: No Action Indicated (NAI), source: FDA, date: September 7, 2010

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