# Amarex Clinical Research, LLC - Inspection Records

Source: https://www.keypedia.com/companies/amarex-clinical-research-llc/1fe4c07b-4ea1-4b76-821c-c20a7e0bfad4

> Inspection records and compliance data for Amarex Clinical Research, LLC in Germantown, Maryland. Access full analysis and detailed observations.

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## Details

- Name: Amarex Clinical Research, LLC
- FEI Number: 3007940998
- City: Germantown
- State: Maryland
- Country Name: United States
- Address Line 1: 20201 Century Blvd Fl 4
- Zip Code: 20874

## Related Documents

- [483 - Amarex Clinical Research, LLC - 2021-12-29](https://www.keypedia.com/records/483/amarex-clinical-research-llc/b91ae07d-9a97-463a-9ca0-968328c6ad61) — source: FDA, date: December 29, 2021
- [FDA Inspection 1160749 - Amarex Clinical Research, LLC - 2021-12-29](https://www.keypedia.com/records/fda_inspections/amarex-clinical-research-llc/80edfba9-eeed-43c3-b32e-9f45d770248f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 29, 2021
- [FDA Inspection 1158863 - Amarex Clinical Research, LLC - 2021-11-03](https://www.keypedia.com/records/fda_inspections/amarex-clinical-research-llc/33c8fc47-645d-4a7a-b617-2f49452530e9) — classification: No Action Indicated (NAI), source: FDA, date: November 3, 2021
- [FDA Inspection 1035083 - Amarex Clinical Research, LLC - 2017-12-05](https://www.keypedia.com/records/fda_inspections/amarex-clinical-research-llc/ad7509b9-ef40-4217-9f61-0deedccbb547) — classification: No Action Indicated (NAI), source: FDA, date: December 5, 2017
- [FDA Inspection 911612 - Amarex Clinical Research, LLC - 2015-01-28](https://www.keypedia.com/records/fda_inspections/amarex-clinical-research-llc/5c99960d-3af6-4b87-acde-eafde197741b) — classification: No Action Indicated (NAI), source: FDA, date: January 28, 2015
- [FDA Inspection 637968 - Amarex Clinical Research, LLC - 2010-01-11](https://www.keypedia.com/records/fda_inspections/amarex-clinical-research-llc/f681dc3d-1ef5-49b4-af94-7ef16e03d272) — classification: No Action Indicated (NAI), source: FDA, date: January 11, 2010

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