# Perryman Company, Houston, PA – FDA Inspections

Source: https://www.keypedia.com/companies/perryman-company/0018ea83-8ef1-4d46-bb8d-aaa94e2e285c

> Inspection records and compliance data for Perryman Company in Houston, Pennsylvania. 4 FDA inspections on record, 1 Form 483, last inspected March 10, 2026.

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## Details

- Name: Perryman Company
- FEI Number: 3009882462
- Address Line 1: 149 S Johnson Rd
- City: Houston
- State: Pennsylvania
- Zip Code: 15342
- Country Name: United States
- Address: 149 S Johnson Rd, Houston, Pennsylvania 15342, United States
- Country: United States

## Related Documents

- [FDA Inspection 1307166 - Perryman Company - 2026-03-10](https://www.keypedia.com/records/fda_inspections/perryman-company/1728517d-3b78-4015-aedb-433f7fbaa9fa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 10, 2026
- FDA Inspection 1307166 - Perryman Company - 2026-03-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 10, 2026
- [483 - Perryman Company - 2019-10-10](https://www.keypedia.com/records/483/perryman-company/7fa5c3c7-235f-4b36-b9aa-f7a8fff541b0) — source: FDA, date: October 10, 2019
- [FDA Inspection 1106963 - Perryman Company - 2019-10-10](https://www.keypedia.com/records/fda_inspections/perryman-company/8efa677d-4e36-4947-84d8-112f9c581481) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 10, 2019
- FDA Inspection 1106963 - Perryman Company - 2019-10-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 10, 2019
- FDA Inspection 1005622 - Perryman Company - 2017-02-09 — classification: No Action Indicated (NAI), source: FDA, date: February 9, 2017
- FDA Inspection 1005622 - Perryman Company - 2017-02-09 — classification: No Action Indicated (NAI), source: FDA, date: February 9, 2017
- FDA Inspection 941493 - Perryman Company - 2015-09-10 — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2015
- FDA Inspection 941493 - Perryman Company - 2015-09-10 — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2015

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