# Weinert Fiber Optics Inc., Williamsburg, VA – FDA Inspections

Source: https://www.keypedia.com/companies/weinert-fiber-optics-inc/eee3b32f-5b0e-467d-9ac9-4535f994303c

> Inspection records and compliance data for Weinert Fiber Optics Inc. in Williamsburg, Virginia. 3 FDA inspections on record, 1 Form 483, last inspected January 13, 2023.

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## Details

- Name: Weinert Fiber Optics Inc.
- FEI Number: 3007336385
- Address Line 1: 209 Bulifants Blvd
- City: Williamsburg
- State: Virginia
- Zip Code: 23188
- Country Name: United States
- Address: 209 Bulifants Blvd, Williamsburg, Virginia 23188, United States
- Country: United States

## Related Documents

- [483 - Weinert Fiber Optics Inc. - 2023-01-13](https://www.keypedia.com/records/483/weinert-fiber-optics-inc/ca553af1-8c7d-410e-b0e4-1fc4e1a85c17) — source: FDA, date: January 13, 2023
- FDA Inspection 1195236 - Weinert Fiber Optics Inc. - 2023-01-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2023
- [FDA Inspection 1195236 - Weinert Fiber Optics Inc. - 2023-01-13](https://www.keypedia.com/records/fda_inspections/weinert-fiber-optics-inc/3a77d1df-1690-4f55-aead-2c6025840e96) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2023
- FDA Inspection 1074745 - Weinert Fiber Optics Inc. - 2018-11-21 — classification: No Action Indicated (NAI), source: FDA, date: November 21, 2018
- FDA Inspection 1074745 - Weinert Fiber Optics Inc. - 2018-11-21 — classification: No Action Indicated (NAI), source: FDA, date: November 21, 2018
- FDA Inspection 1074745 - Weinert Fiber Optics Inc. - 2018-11-21 — classification: No Action Indicated (NAI), source: FDA, date: November 21, 2018
- FDA Inspection 980868 - Weinert Fiber Optics Inc. - 2016-08-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 10, 2016
- [FDA Inspection 980868 - Weinert Fiber Optics Inc. - 2016-08-10](https://www.keypedia.com/records/fda_inspections/weinert-fiber-optics-inc/b4546e9a-81bb-4b08-996e-488bc55753c8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 10, 2016

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