# Orthodent Laboratory, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/orthodent-laboratory-inc/9b8304f9-d206-4b2d-89a4-a029f14e1c72

> Inspection records and compliance data for Orthodent Laboratory, Inc. in Buffalo, New York. Access full analysis and detailed observations.

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## Details

- Name: Orthodent Laboratory, Inc.
- FEI Number: 3015421090
- City: Buffalo
- State: New York
- Country Name: United States
- Address Line 1: 155 Chandler St
- Zip Code: 14207

## Related Documents

- [483 - Orthodent Laboratory, Inc. - 2023-11-13](https://www.keypedia.com/records/483/orthodent-laboratory-inc/fd9bea80-79a8-46fe-a695-cd171d7a09ef) — source: FDA, date: November 13, 2023
- [FDA Inspection 1223196 - Orthodent Laboratory, Inc. - 2023-11-13](https://www.keypedia.com/records/fda_inspections/orthodent-laboratory-inc/0bd84701-1ee9-43ef-8223-f0e668d9998d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 13, 2023
- [FDA Inspection 1223196 - Orthodent Laboratory, Inc. - 2023-11-13](https://www.keypedia.com/records/fda_inspections/orthodent-laboratory-inc/89255fb1-7f40-4f81-bcc9-e523a705f75f) — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2023
- [483 - Orthodent Laboratory, Inc. - 2021-03-24](https://www.keypedia.com/records/483/orthodent-laboratory-inc/1b39cdfc-657c-497e-962f-767aae5e0b8b) — source: FDA, date: March 24, 2021
- [EIR - Orthodent Laboratory, Inc. - 2021-03-24](https://www.keypedia.com/records/eir/orthodent-laboratory-inc/c4f1684d-f2dd-470c-b8ff-e40b98b36f6c) — source: FDA, date: March 24, 2021
- [FDA Inspection 1137122 - Orthodent Laboratory, Inc. - 2021-03-24](https://www.keypedia.com/records/fda_inspections/orthodent-laboratory-inc/f9f50106-2197-4b4b-a609-329d5de1f5de) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 24, 2021
- [FDA Inspection 1137122 - Orthodent Laboratory, Inc. - 2021-03-24](https://www.keypedia.com/records/fda_inspections/orthodent-laboratory-inc/e992289f-a30e-4d3a-b354-8f162a791d41) — classification: No Action Indicated (NAI), source: FDA, date: March 24, 2021

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