# FDA Inspection 1204662 - Anesthetic Gas Reclamation Inc. - May 04, 2023

Source: https://www.keypedia.com/records/fda_inspections/anesthetic-gas-reclamation-inc/58c10046-ce09-488f-87a2-63c480cf43fb
Source feed: FDA_Inspections

> FDA Inspection 1204662 for Anesthetic Gas Reclamation Inc. on May 04, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1204662
- Company Name: Anesthetic Gas Reclamation Inc.
- Inspection Date: 2023-05-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1204662 - 2023-05-04](https://www.keypedia.com/records/fda_inspections/anesthetic-gas-reclamation-inc/48d3014c-5568-4a0c-9003-d396680bfc6b)
- [FDA Inspection 1061728 - 2018-08-09](https://www.keypedia.com/records/fda_inspections/anesthetic-gas-reclamation-inc/e842dfce-4383-4bea-a17a-13fb69977766)
- [FDA Inspection 1061728 - 2018-08-09](https://www.keypedia.com/records/fda_inspections/anesthetic-gas-reclamation-inc/13131b82-509b-4a04-8aa6-6d638b51deb7)
- [FDA Inspection 716653 - 2011-03-15](https://www.keypedia.com/records/fda_inspections/anesthetic-gas-reclamation-inc/09b97cef-81de-4339-abfa-afc73af358d5)

Company: https://www.keypedia.com/companies/anesthetic-gas-reclamation-inc/e3eea8ec-b6d1-4355-b094-441caf3e12ab

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7