# Stockton Graham & Company, Raleigh, NC – FDA Inspections

Source: https://www.keypedia.com/companies/stockton-graham-company/0a59d6e9-beb3-4b50-b9cc-1a1a9a88ab0e

> Inspection records and compliance data for Stockton Graham & Company in Raleigh, North Carolina. 6 FDA inspections on record, 1 Form 483, last inspected March 12, 2024.

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## Details

- Name: Stockton Graham & Company
- FEI Number: 3004399247
- Address Line 1: 4320 Delta Lake Dr
- City: Raleigh
- State: North Carolina
- Zip Code: 27612
- Country Name: United States
- Address: 4320 Delta Lake Dr, Raleigh, North Carolina 27612, United States
- Country: United States

## Related Documents

- FDA Inspection 1234775 - Stockton Graham & Company - 2024-03-12 — source: FDA, date: March 12, 2024
- FDA Inspection 1169827 - Stockton Graham & Company - 2022-05-16 — classification: No Action Indicated (NAI), source: FDA, date: May 16, 2022
- [FDA Inspection 1019765 - Stockton Graham & Company - 2017-07-11](https://www.keypedia.com/records/fda_inspections/stockton-graham-company/7c0e070b-4363-4905-adc8-e0f38f01305d) — source: FDA, date: July 11, 2017
- FDA Inspection 902864 - Stockton Graham & Company - 2014-10-16 — classification: No Action Indicated (NAI), source: FDA, date: October 16, 2014
- [FDA Inspection 894481 - Stockton Graham & Company - 2014-08-28](https://www.keypedia.com/records/fda_inspections/stockton-graham-company/a72067e9-1caa-473b-82c9-a21d8095d0b3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 28, 2014
- FDA Inspection 671632 - Stockton Graham & Company - 2010-07-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 14, 2010
- [FDA Inspection 671632 - Stockton Graham & Company - 2010-07-14](https://www.keypedia.com/records/fda_inspections/stockton-graham-company/c13f99ce-6eeb-4ef1-8f47-a5b50b1a162d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 14, 2010
- FDA Inspection 671632 - Stockton Graham & Company - 2010-07-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 14, 2010

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