# Avara Aiken Pharmaceutical Services Inc., Aiken, SC – FDA Inspections

Source: https://www.keypedia.com/companies/avara-aiken-pharmaceutical-services-inc/b0a8f671-a1e3-4d57-9e6c-1eab2d17e5a1

> Inspection records and compliance data for Avara Aiken Pharmaceutical Services Inc. in Aiken, South Carolina. 5 FDA inspections on record, last inspected July 10, 2015.

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## Details

- Name: Avara Aiken Pharmaceutical Services Inc.
- FEI Number: 1046838
- Address Line 1: 65 Windham Blvd
- City: Aiken
- State: South Carolina
- Zip Code: 29805
- Country Name: United States
- Address: 65 Windham Blvd, Aiken, South Carolina 29805, United States
- Country: United States

## Related Documents

- [FDA Inspection 933389 - Avara Aiken Pharmaceutical Services Inc. - 2015-07-10](https://www.keypedia.com/records/fda_inspections/avara-aiken-pharmaceutical-services-inc/7286a456-ff56-48b7-b73b-6701d48dbd8e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 10, 2015
- FDA Inspection 765141 - Avara Aiken Pharmaceutical Services Inc. - 2012-01-27 — classification: No Action Indicated (NAI), source: FDA, date: January 27, 2012
- FDA Inspection 765141 - Avara Aiken Pharmaceutical Services Inc. - 2012-01-27 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 27, 2012
- FDA Inspection 717226 - Avara Aiken Pharmaceutical Services Inc. - 2011-01-27 — classification: No Action Indicated (NAI), source: FDA, date: January 27, 2011
- FDA Inspection 659478 - Avara Aiken Pharmaceutical Services Inc. - 2010-04-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 19, 2010
- [FDA Inspection 659478 - Avara Aiken Pharmaceutical Services Inc. - 2010-04-19](https://www.keypedia.com/records/fda_inspections/avara-aiken-pharmaceutical-services-inc/bf836b3b-61c9-4903-ae1f-3d1b0cb49cf9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 19, 2010
- FDA Inspection 547658 - Avara Aiken Pharmaceutical Services Inc. - 2008-11-07 — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2008

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