# The A.R.T. Institute of Washington, Inc., Bethesda, MD – FDA Inspections

Source: https://www.keypedia.com/companies/the-art-institute-of-washington-inc/e6e87941-e5a2-4b8d-8e81-033ed17785a4

> Inspection records and compliance data for The A.R.T. Institute of Washington, Inc. in Bethesda, Maryland. 5 FDA inspections on record, last inspected June 08, 2022.

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## Details

- Name: The A.R.T. Institute of Washington, Inc.
- FEI Number: 3003939193
- Address Line 1: 8901 Wisconsin Ave, Bldg. 10, 2nd Floor, Dept. Arc, Rm 2104
- City: Bethesda
- State: Maryland
- Zip Code: 20889
- Country Name: United States
- Address: 8901 Wisconsin Ave, Bldg. 10, 2nd Floor, Dept. Arc, Rm 2104, Bethesda, Maryland 20889, United States
- Country: United States

## Related Documents

- [483 - The A.R.T. Institute of Washington, Inc. - 2022-06-08](https://www.keypedia.com/records/483/the-art-institute-of-washington-inc/750f9eb0-54f4-4565-882e-fb5540a8ce36) — source: FDA, date: June 8, 2022
- FDA Inspection 1171293 - The A.R.T. Institute of Washington, Inc. - 2022-06-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 8, 2022
- FDA Inspection 1171293 - The A.R.T. Institute of Washington, Inc. - 2022-06-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 8, 2022
- FDA Inspection 1171293 - The A.R.T. Institute of Washington, Inc. - 2022-06-08 — classification: No Action Indicated (NAI), source: FDA, date: June 8, 2022
- FDA Inspection 1072158 - The A.R.T. Institute of Washington, Inc. - 2018-10-11 — classification: No Action Indicated (NAI), source: FDA, date: October 11, 2018
- FDA Inspection 945691 - The A.R.T. Institute of Washington, Inc. - 2015-10-13 — classification: No Action Indicated (NAI), source: FDA, date: October 13, 2015
- FDA Inspection 798982 - The A.R.T. Institute of Washington, Inc. - 2012-09-13 — classification: No Action Indicated (NAI), source: FDA, date: September 13, 2012
- FDA Inspection 652899 - The A.R.T. Institute of Washington, Inc. - 2010-03-17 — classification: No Action Indicated (NAI), source: FDA, date: March 17, 2010

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