# Pharma Packaging Solutions, LLC dba TJOAPACK, LLC, Clinton, TN – FDA Inspections

Source: https://www.keypedia.com/companies/pharma-packaging-solutions-llc-dba-tjoapack-llc/724861b2-9b0e-4b90-845a-4b6e811661fa

> Inspection records and compliance data for Pharma Packaging Solutions, LLC dba TJOAPACK, LLC in Clinton, Tennessee. 5 FDA inspections on record, last inspected June 28, 2023.

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## Details

- Name: Pharma Packaging Solutions, LLC dba TJOAPACK, LLC
- FEI Number: 3002763532
- Business Operations: PACK, REPACK
- Address Line 1: 341 Jd Yarnell Industrial Pkwy
- City: Clinton
- State: Tennessee
- Zip Code: 37716
- Country Name: United States
- Address: 341 Jd Yarnell Industrial Pkwy, Clinton, Tennessee 37716, United States
- Country: United States

## Related Documents

- FDA Inspection 1209725 - Pharma Packaging Solutions, LLC dba TJOAPACK, LLC - 2023-06-28 — classification: No Action Indicated (NAI), source: FDA, date: June 28, 2023
- FDA Inspection 1196856 - Pharma Packaging Solutions, LLC dba TJOAPACK, LLC - 2023-01-19 — classification: No Action Indicated (NAI), source: FDA, date: January 19, 2023
- FDA Inspection 1196856 - Pharma Packaging Solutions, LLC dba TJOAPACK, LLC - 2023-01-19 — classification: No Action Indicated (NAI), source: FDA, date: January 19, 2023
- FDA Inspection 933511 - Pharma Packaging Solutions, LLC dba TJOAPACK, LLC - 2015-07-08 — classification: No Action Indicated (NAI), source: FDA, date: July 8, 2015
- [FDA Inspection 848858 - Pharma Packaging Solutions, LLC dba TJOAPACK, LLC - 2013-09-18](https://www.keypedia.com/records/fda_inspections/pharma-packaging-solutions-llc-dba-tjoapack-llc/63002fb6-8935-4a17-8aaf-265c967be45d) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2013
- FDA Inspection 634974 - Pharma Packaging Solutions, LLC dba TJOAPACK, LLC - 2009-11-19 — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2009
- FDA Inspection 634974 - Pharma Packaging Solutions, LLC dba TJOAPACK, LLC - 2009-11-19 — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2009

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