# K. W. Griffen Company DBA Biomed Packaging Systems - Inspection Records

Source: https://www.keypedia.com/companies/k-w-griffen-company-dba-biomed-packaging-systems/4f4e6ca6-e91b-44e7-a5d1-52537169f3a4

> Inspection records and compliance data for K. W. Griffen Company DBA Biomed Packaging Systems in Norwalk, Connecticut. Access full analysis and detailed observations.

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## Details

- Name: K. W. Griffen Company DBA Biomed Packaging Systems
- FEI Number: 1211177
- City: Norwalk
- State: Connecticut
- Country Name: United States
- Address Line 1: 100 Pearl St
- Zip Code: 06850

## Related Documents

- [483 - K. W. Griffen Company DBA Biomed Packaging Systems - 2025-05-16](https://www.keypedia.com/records/483/k-w-griffen-company-dba-biomed-packaging-systems/5977ed6b-9563-41fe-a227-f51daac56f4a) — source: FDA, date: May 16, 2025
- [FDA Inspection 1270809 - K. W. Griffen Company DBA Biomed Packaging Systems - 2025-05-16](https://www.keypedia.com/records/fda_inspections/k-w-griffen-company-dba-biomed-packaging-systems/68ceebac-77ef-43b9-9736-91329febb91e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 16, 2025
- [483 - K. W. Griffen Company DBA Biomed Packaging Systems - 2024-03-15](https://www.keypedia.com/records/483/k-w-griffen-company-dba-biomed-packaging-systems/3512597a-e8ba-4098-a378-a0a8dfbe25c5) — source: FDA, date: March 15, 2024
- [FDA Inspection 1232979 - K. W. Griffen Company DBA Biomed Packaging Systems - 2024-03-15](https://www.keypedia.com/records/fda_inspections/k-w-griffen-company-dba-biomed-packaging-systems/545b8e3b-e17f-473a-9285-fbb36fc03724) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 15, 2024
- [FDA Inspection 1062093 - K. W. Griffen Company DBA Biomed Packaging Systems - 2018-08-14](https://www.keypedia.com/records/fda_inspections/k-w-griffen-company-dba-biomed-packaging-systems/222439c1-91f2-4638-ab8d-5bc763091cc5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 14, 2018
- [FDA Inspection 771859 - K. W. Griffen Company DBA Biomed Packaging Systems - 2012-02-28](https://www.keypedia.com/records/fda_inspections/k-w-griffen-company-dba-biomed-packaging-systems/f74a0988-4c33-4313-8595-b1015a2cf300) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 28, 2012
- [FDA Inspection 698666 - K. W. Griffen Company DBA Biomed Packaging Systems - 2010-11-18](https://www.keypedia.com/records/fda_inspections/k-w-griffen-company-dba-biomed-packaging-systems/e2d28640-21b0-4086-9449-ad5cfcc46978) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 18, 2010
- [FDA Inspection 698666 - K. W. Griffen Company DBA Biomed Packaging Systems - 2010-11-18](https://www.keypedia.com/records/fda_inspections/k-w-griffen-company-dba-biomed-packaging-systems/a4957ac5-d51c-45cf-bdb2-83242fbbac3a) — classification: No Action Indicated (NAI), source: FDA, date: November 18, 2010
- [FDA Inspection 630664 - K. W. Griffen Company DBA Biomed Packaging Systems - 2009-11-09](https://www.keypedia.com/records/fda_inspections/k-w-griffen-company-dba-biomed-packaging-systems/a6e7a822-a331-4ffe-bef7-9aa2d055ea25) — classification: No Action Indicated (NAI), source: FDA, date: November 9, 2009
- [FDA Inspection 630664 - K. W. Griffen Company DBA Biomed Packaging Systems - 2009-11-09](https://www.keypedia.com/records/fda_inspections/k-w-griffen-company-dba-biomed-packaging-systems/1ff871b7-89e5-42e9-a46e-ef95e4f804e0) — classification: No Action Indicated (NAI), source: FDA, date: November 9, 2009

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