# e+ OncoLogics Louisiana, LLC, Lafayette, LA – FDA Inspections

Source: https://www.keypedia.com/companies/e-oncologics-louisiana-llc/039f426a-8dbf-437e-aab0-a182d41dc4b5

> Inspection records and compliance data for e+ OncoLogics Louisiana, LLC in Lafayette, Louisiana. 8 FDA inspections on record, last inspected July 09, 2024.

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## Details

- Name: e+ OncoLogics Louisiana, LLC
- FEI Number: 1000306891
- Address Line 1: 4809 Ambassador Caffery Pkwy Ste 100
- City: Lafayette
- State: Louisiana
- Zip Code: 70508
- Country Name: United States
- Address: 4809 Ambassador Caffery Pkwy Ste 100, Lafayette, Louisiana 70508, United States
- Country: United States

## Related Documents

- [FDA Inspection 1245125 - e+ OncoLogics Louisiana, LLC - 2024-07-09](https://www.keypedia.com/records/fda_inspections/e-oncologics-louisiana-llc/8c5ba84c-740c-47d1-b0bc-813b41d85a52) — classification: No Action Indicated (NAI), source: FDA, date: July 9, 2024
- FDA Inspection 1171284 - e+ OncoLogics Louisiana, LLC - 2022-03-28 — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2022
- FDA Inspection 1171284 - e+ OncoLogics Louisiana, LLC - 2022-03-28 — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2022
- FDA Inspection 1046033 - e+ OncoLogics Louisiana, LLC - 2018-01-18 — classification: No Action Indicated (NAI), source: FDA, date: January 18, 2018
- FDA Inspection 977278 - e+ OncoLogics Louisiana, LLC - 2016-07-21 — classification: No Action Indicated (NAI), source: FDA, date: July 21, 2016
- FDA Inspection 907097 - e+ OncoLogics Louisiana, LLC - 2014-12-15 — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2014
- FDA Inspection 833821 - e+ OncoLogics Louisiana, LLC - 2013-05-31 — classification: No Action Indicated (NAI), source: FDA, date: May 31, 2013
- FDA Inspection 746593 - e+ OncoLogics Louisiana, LLC - 2011-09-15 — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2011
- FDA Inspection 665882 - e+ OncoLogics Louisiana, LLC - 2010-05-26 — classification: No Action Indicated (NAI), source: FDA, date: May 26, 2010

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