# Avery Biomedical Devices, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/avery-biomedical-devices-inc/d8b8209f-40b0-48d3-94a0-30333f988c0d

> Inspection records and compliance data for Avery Biomedical Devices, Inc. in Commack, New York. Access full analysis and detailed observations.

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## Details

- Name: Avery Biomedical Devices, Inc.
- FEI Number: 2427696
- City: Commack
- State: New York
- Country Name: United States
- Address Line 1: 61 Mall Dr
- Zip Code: 11725

## Related Documents

- [FDA Inspection 1256891 - Avery Biomedical Devices, Inc. - 2024-10-30](https://www.globalkeysolutions.net/records/fda_inspections/avery-biomedical-devices-inc/f8c745f5-8175-433e-9726-01f936e6db75) — source: FDA, date: October 30, 2024
- [FDA Inspection 1256891 - Avery Biomedical Devices, Inc. - 2024-10-30](https://www.globalkeysolutions.net/records/fda_inspections/avery-biomedical-devices-inc/8e703252-c62d-4e7f-b71d-147fc0dc0057) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2024
- [FDA Inspection 1256891 - Avery Biomedical Devices, Inc. - 2024-10-30](https://www.globalkeysolutions.net/records/fda_inspections/avery-biomedical-devices-inc/0152c9f3-c0a2-4650-b5f5-6398c50e89f4) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2024
- [FDA Inspection 1167847 - Avery Biomedical Devices, Inc. - 2022-04-14](https://www.globalkeysolutions.net/records/fda_inspections/avery-biomedical-devices-inc/b032b304-aac3-457e-be38-2e6b43849b3d) — classification: No Action Indicated (NAI), source: FDA, date: April 14, 2022
- [FDA Inspection 1167847 - Avery Biomedical Devices, Inc. - 2022-04-14](https://www.globalkeysolutions.net/records/fda_inspections/avery-biomedical-devices-inc/44c149b8-0142-4a82-923a-993b1c0407d5) — classification: No Action Indicated (NAI), source: FDA, date: April 14, 2022
- [483 - Avery Biomedical Devices, Inc. - 2019-07-16](https://www.globalkeysolutions.net/records/483/avery-biomedical-devices-inc/630b21c7-014c-4a81-b4f3-8d111465b54f) — source: FDA, date: July 16, 2019
- [FDA Inspection 1096555 - Avery Biomedical Devices, Inc. - 2019-07-16](https://www.globalkeysolutions.net/records/fda_inspections/avery-biomedical-devices-inc/9a2e35d3-6fd5-4296-8993-921c6336db31) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 16, 2019
- [FDA Inspection 1096555 - Avery Biomedical Devices, Inc. - 2019-07-16](https://www.globalkeysolutions.net/records/fda_inspections/avery-biomedical-devices-inc/fa3349c0-0b72-4da1-bf39-99d078d6a011) — classification: No Action Indicated (NAI), source: FDA, date: July 16, 2019
- [483 - Avery Biomedical Devices, Inc. - 2017-04-17](https://www.globalkeysolutions.net/records/483/avery-biomedical-devices-inc/2d5194de-4889-48d0-ab21-7fa0fd9500da) — source: FDA, date: April 17, 2017
- [FDA Inspection 1008035 - Avery Biomedical Devices, Inc. - 2017-04-17](https://www.globalkeysolutions.net/records/fda_inspections/avery-biomedical-devices-inc/8e123d7d-9a73-4880-8510-4ca9347e52ce) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 17, 2017
- [FDA Inspection 972473 - Avery Biomedical Devices, Inc. - 2016-03-24](https://www.globalkeysolutions.net/records/fda_inspections/avery-biomedical-devices-inc/9f8499f9-530b-4092-87bf-38d1dccfc532) — classification: No Action Indicated (NAI), source: FDA, date: March 24, 2016
- [FDA Inspection 972473 - Avery Biomedical Devices, Inc. - 2016-03-24](https://www.globalkeysolutions.net/records/fda_inspections/avery-biomedical-devices-inc/882e8f18-1d54-40dd-8649-b4f07ad595ed) — classification: No Action Indicated (NAI), source: FDA, date: March 24, 2016

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