# Accupac, LLC, Mainland, PA – FDA Inspections

Source: https://www.keypedia.com/companies/accupac-llc/89921980-5d45-47e3-8098-b5700be9f082

> Inspection records and compliance data for Accupac, LLC in Mainland, Pennsylvania. 5 FDA inspections on record, 1 Form 483, last inspected January 24, 2023.

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## Details

- Name: Accupac, LLC
- FEI Number: 2518467
- Address Line 1: 1501 Industrial Boulevard
- City: Mainland
- State: Pennsylvania
- Zip Code: 19451
- Country Name: United States
- Address: 1501 Industrial Boulevard, Mainland, Pennsylvania 19451, United States
- Country: United States

## Related Documents

- FDA Inspection 1196516 - Accupac, LLC - 2023-01-24 — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2023
- FDA Inspection 1196516 - Accupac, LLC - 2023-01-24 — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2023
- [FDA Inspection 1030873 - Accupac, LLC - 2017-11-02](https://www.keypedia.com/records/fda_inspections/accupac-llc/fd419061-07d8-4e57-aba1-a4307fcafd33) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 2, 2017
- FDA Inspection 1030873 - Accupac, LLC - 2017-11-02 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 2, 2017
- FDA Inspection 986007 - Accupac, LLC - 2016-03-31 — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2016
- FDA Inspection 986007 - Accupac, LLC - 2016-03-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 31, 2016
- FDA Inspection 986007 - Accupac, LLC - 2016-03-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 31, 2016
- FDA Inspection 986007 - Accupac, LLC - 2016-03-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 31, 2016
- FDA Inspection 844740 - Accupac, LLC - 2013-07-19 — classification: No Action Indicated (NAI), source: FDA, date: July 19, 2013
- FDA Inspection 844740 - Accupac, LLC - 2013-07-19 — classification: No Action Indicated (NAI), source: FDA, date: July 19, 2013

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