# Woodbine Products Company, Medina, OH – FDA Inspections

Source: https://www.keypedia.com/companies/woodbine-products-company/b7fae119-8c1a-44b5-b3ce-11c0750b7689

> Inspection records and compliance data for Woodbine Products Company in Medina, Ohio. 5 FDA inspections on record, 1 Form 483, 1 warning letter, last inspected February 13, 2026.

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## Details

- Name: Woodbine Products Company
- FEI Number: 1519202
- Address Line 1: 915 W Smith Rd
- City: Medina
- State: Ohio
- Zip Code: 44256
- Country Name: United States
- Address: 915 W Smith Rd, Medina, Ohio 44256, United States
- Country: United States

## Related Documents

- [WARNING_LETTER - Woodbine Products Company - 2026-02-13](https://www.keypedia.com/records/warning_letter/woodbine-products-company/fb5e6617-379e-4ff7-b43f-325b2d8e24bf) — source: FDA, date: February 13, 2026
- [483 - Woodbine Products Company - 2026-02-13](https://www.keypedia.com/records/483/woodbine-products-company/d7f3fdff-8e64-4c56-ae6d-47de65c4c5fe) — source: FDA, date: February 13, 2026
- [FDA Inspection 1303082 - Woodbine Products Company - 2026-02-13](https://www.keypedia.com/records/fda_inspections/woodbine-products-company/a90c2669-1f13-4831-8c4d-75450030a688) — source: FDA, date: February 13, 2026
- [483 - Woodbine Products Company - 2022-09-01](https://www.keypedia.com/records/483/woodbine-products-company/57ad6207-e0e2-4dc8-be24-daffd84d195f) — source: FDA, date: September 1, 2022
- FDA Inspection 1179797 - Woodbine Products Company - 2022-09-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 1, 2022
- [FDA Inspection 985003 - Woodbine Products Company - 2016-09-06](https://www.keypedia.com/records/fda_inspections/woodbine-products-company/fd85a7ba-c272-4184-817d-f4e3632e4afe) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 6, 2016
- FDA Inspection 749084 - Woodbine Products Company - 2011-10-20 — classification: No Action Indicated (NAI), source: FDA, date: October 20, 2011
- FDA Inspection 636524 - Woodbine Products Company - 2009-12-16 — classification: No Action Indicated (NAI), source: FDA, date: December 16, 2009

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