# Analogic Corporation - Inspection Records

Source: https://www.keypedia.com/companies/analogic-corporation/e833b34e-cb3b-4b19-ac2f-8ae91b12d33f

> Inspection records and compliance data for Analogic Corporation in Peabody, Massachusetts. Access full analysis and detailed observations.

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## Details

- Name: Analogic Corporation
- FEI Number: 1220672
- City: Peabody
- State: Massachusetts
- Country Name: United States
- Address Line 1: 8 Centennial Dr
- Zip Code: 01960

## Related Documents

- [483 - Analogic Corporation - 2022-08-25](https://www.keypedia.com/records/483/analogic-corporation/9f763be6-0aca-436e-9e88-c821fdcda99f) — source: FDA, date: August 25, 2022
- [FDA Inspection 1178325 - Analogic Corporation - 2022-08-25](https://www.keypedia.com/records/fda_inspections/analogic-corporation/c3f15065-1d2b-4471-8f55-b4d423bb7d26) — classification: No Action Indicated (NAI), source: FDA, date: August 25, 2022
- [FDA Inspection 1178325 - Analogic Corporation - 2022-08-25](https://www.keypedia.com/records/fda_inspections/analogic-corporation/d2a225b0-b5b0-4e30-9848-bbe92b473396) — classification: No Action Indicated (NAI), source: FDA, date: August 25, 2022
- [FDA Inspection 1178325 - Analogic Corporation - 2022-08-25](https://www.keypedia.com/records/fda_inspections/analogic-corporation/65ab08b1-7df8-478f-890b-8b2fa03c8596) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 25, 2022
- [FDA Inspection 1109873 - Analogic Corporation - 2019-11-04](https://www.keypedia.com/records/fda_inspections/analogic-corporation/c3ac90eb-2abb-4b13-996b-d3b0aaf76cac) — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2019
- [FDA Inspection 1109873 - Analogic Corporation - 2019-11-04](https://www.keypedia.com/records/fda_inspections/analogic-corporation/567b09e9-2f49-46fd-858c-e5ea5401fad3) — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2019
- [FDA Inspection 1109873 - Analogic Corporation - 2019-11-04](https://www.keypedia.com/records/fda_inspections/analogic-corporation/ad1ba073-f701-4079-b1e8-f9066aaf658a) — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2019
- [FDA Inspection 1011463 - Analogic Corporation - 2017-05-17](https://www.keypedia.com/records/fda_inspections/analogic-corporation/7fc05571-6110-4ef9-9c97-a00c30a58d85) — classification: No Action Indicated (NAI), source: FDA, date: May 17, 2017
- [FDA Inspection 1011463 - Analogic Corporation - 2017-05-17](https://www.keypedia.com/records/fda_inspections/analogic-corporation/f3379949-103c-4416-912f-a35545e16798) — classification: No Action Indicated (NAI), source: FDA, date: May 17, 2017
- [FDA Inspection 1011463 - Analogic Corporation - 2017-05-17](https://www.keypedia.com/records/fda_inspections/analogic-corporation/9bc92674-0121-485a-a439-556cd97bef74) — classification: No Action Indicated (NAI), source: FDA, date: May 17, 2017
- [FDA Inspection 895141 - Analogic Corporation - 2014-09-04](https://www.keypedia.com/records/fda_inspections/analogic-corporation/a3ee7e5a-bd61-4248-bdec-23ce8a8e8764) — classification: No Action Indicated (NAI), source: FDA, date: September 4, 2014

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