# ProCore Pharma, LLC, Coppell, TX – FDA Inspections

Source: https://www.keypedia.com/companies/procore-pharma-llc/e3e8d66c-0774-4480-ae06-6cfc2d7f7ec0

> Inspection records and compliance data for ProCore Pharma, LLC in Coppell, Texas. 3 FDA inspections on record (1 OAI), last inspected June 26, 2013.

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## Details

- Name: ProCore Pharma, LLC
- FEI Number: 3010165198
- Address Line 1: 1025 S Belt Line Rd Ste 100
- City: Coppell
- State: Texas
- Zip Code: 75019
- Country Name: United States
- Address: 1025 S Belt Line Rd Ste 100, Coppell, Texas 75019, United States
- Country: United States

## Related Documents

- FDA Inspection 844207 - ProCore Pharma, LLC - 2013-06-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 26, 2013
- FDA Inspection 844207 - ProCore Pharma, LLC - 2013-06-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 26, 2013
- FDA Inspection 844207 - ProCore Pharma, LLC - 2013-06-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 26, 2013
- FDA Inspection 844207 - ProCore Pharma, LLC - 2013-06-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 26, 2013
- FDA Inspection 742077 - ProCore Pharma, LLC - 2011-09-08 — classification: Official Action Indicated (OAI), source: FDA, date: September 8, 2011
- [FDA Inspection 742077 - ProCore Pharma, LLC - 2011-09-08](https://www.keypedia.com/records/fda_inspections/procore-pharma-llc/c72ac474-df0d-4035-a7d6-c0e2cbfbeb54) — classification: Official Action Indicated (OAI), source: FDA, date: September 8, 2011
- FDA Inspection 742077 - ProCore Pharma, LLC - 2011-09-08 — classification: Official Action Indicated (OAI), source: FDA, date: September 8, 2011
- [FDA Inspection 582249 - ProCore Pharma, LLC - 2009-05-04](https://www.keypedia.com/records/fda_inspections/procore-pharma-llc/b1d27e58-3ffb-4e53-a525-4b4bff5c9285) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 4, 2009
- FDA Inspection 582249 - ProCore Pharma, LLC - 2009-05-04 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 4, 2009

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