# Pepper Source Limited - Inspection Records

Source: https://www.globalkeysolutions.net/companies/pepper-source-limited/8b476be1-a13c-41da-9af9-edff07ce9efc

> Inspection records and compliance data for Pepper Source Limited in Van Buren, Arkansas. Access full analysis and detailed observations.

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## Details

- Name: Pepper Source Limited
- FEI Number: 1000220560
- City: Van Buren
- State: Arkansas
- Country Name: United States
- Address Line 1: 5800 Alma Hwy
- Zip Code: 72956

## Related Documents

- [FDA Inspection 1119849 - Pepper Source Limited - 2020-02-07](https://www.globalkeysolutions.net/records/fda_inspections/pepper-source-limited/f3718987-c686-4441-9713-fb07555ef2ca) — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2020
- [FDA Inspection 1026380 - Pepper Source Limited - 2017-08-30](https://www.globalkeysolutions.net/records/fda_inspections/pepper-source-limited/48f41138-b1e6-47bb-bd9b-53ad93dccca9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 30, 2017
- [FDA Inspection 861835 - Pepper Source Limited - 2013-12-20](https://www.globalkeysolutions.net/records/fda_inspections/pepper-source-limited/b7a873cb-c3b1-40f7-9031-3118a41810a1) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2013
- [FDA Inspection 861798 - Pepper Source Limited - 2013-12-20](https://www.globalkeysolutions.net/records/fda_inspections/pepper-source-limited/ba472b82-76ca-411a-8385-aec146af6b5a) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2013
- [FDA Inspection 755642 - Pepper Source Limited - 2011-11-02](https://www.globalkeysolutions.net/records/fda_inspections/pepper-source-limited/4f654023-e8b5-4a32-90e2-d4e6f10984f1) — classification: No Action Indicated (NAI), source: FDA, date: November 2, 2011
- [FDA Inspection 660062 - Pepper Source Limited - 2010-04-08](https://www.globalkeysolutions.net/records/fda_inspections/pepper-source-limited/f5854ef9-f060-4b2c-8ff5-6b5a10753503) — classification: No Action Indicated (NAI), source: FDA, date: April 8, 2010

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