# Yarnall's Inc., Coplay, PA – FDA Inspections

Source: https://www.keypedia.com/companies/yarnalls-inc/30618a77-9436-41e7-b321-80738e46c57d

> Inspection records and compliance data for Yarnall's Inc. in Coplay, Pennsylvania. 8 FDA inspections on record, 1 Form 483, last inspected July 14, 2025.

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## Details

- Name: Yarnall's Inc.
- FEI Number: 3004062924
- Address Line 1: 4343 Hillside Rd
- City: Coplay
- State: Pennsylvania
- Zip Code: 18037
- Country Name: United States
- Address: 4343 Hillside Rd, Coplay, Pennsylvania 18037, United States
- Country: United States

## Related Documents

- FDA Inspection 1275633 - Yarnall's Inc. - 2025-07-14 — source: FDA, date: July 14, 2025
- [FDA Inspection 1275633 - Yarnall's Inc. - 2025-07-14](https://www.keypedia.com/records/fda_inspections/yarnalls-inc/9658e3ab-885b-4285-8dfd-653f9ac9960d) — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2025
- FDA Inspection 1180288 - Yarnall's Inc. - 2022-09-15 — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2022
- [FDA Inspection 1054643 - Yarnall's Inc. - 2018-06-07](https://www.keypedia.com/records/fda_inspections/yarnalls-inc/2f5dda80-4914-4ab9-800c-3a68cd6be1ba) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 7, 2018
- FDA Inspection 930110 - Yarnall's Inc. - 2015-06-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 11, 2015
- FDA Inspection 811231 - Yarnall's Inc. - 2012-12-18 — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2012
- [FDA Inspection 714130 - Yarnall's Inc. - 2011-03-15](https://www.keypedia.com/records/fda_inspections/yarnalls-inc/f6382637-740d-4123-9833-b35b78be3606) — classification: No Action Indicated (NAI), source: FDA, date: March 15, 2011
- FDA Inspection 650899 - Yarnall's Inc. - 2010-03-09 — classification: No Action Indicated (NAI), source: FDA, date: March 9, 2010
- FDA Inspection 561141 - Yarnall's Inc. - 2009-02-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 6, 2009

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