# Anna Jaques Hospital Laboratory, Newburyport, MA – FDA Inspections

Source: https://www.keypedia.com/companies/anna-jaques-hospital-laboratory/aecbd788-052c-4406-ab5e-2f4e50197abf

> Inspection records and compliance data for Anna Jaques Hospital Laboratory in Newburyport, Massachusetts. 7 FDA inspections on record, last inspected July 26, 2022.

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## Details

- Name: Anna Jaques Hospital Laboratory
- FEI Number: 1270660
- Address Line 1: 25 Highland Ave
- City: Newburyport
- State: Massachusetts
- Zip Code: 01950
- Country Name: United States
- Address: 25 Highland Ave, Newburyport, Massachusetts 01950, United States
- Country: United States

## Related Documents

- FDA Inspection 1177226 - Anna Jaques Hospital Laboratory - 2022-07-26 — classification: No Action Indicated (NAI), source: FDA, date: July 26, 2022
- FDA Inspection 1177226 - Anna Jaques Hospital Laboratory - 2022-07-26 — classification: No Action Indicated (NAI), source: FDA, date: July 26, 2022
- FDA Inspection 1076540 - Anna Jaques Hospital Laboratory - 2018-12-10 — classification: No Action Indicated (NAI), source: FDA, date: December 10, 2018
- FDA Inspection 998359 - Anna Jaques Hospital Laboratory - 2017-01-19 — classification: No Action Indicated (NAI), source: FDA, date: January 19, 2017
- [FDA Inspection 907802 - Anna Jaques Hospital Laboratory - 2014-12-15](https://www.keypedia.com/records/fda_inspections/anna-jaques-hospital-laboratory/1c7cb331-9f2c-43f3-b92a-2338de7ff616) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 15, 2014
- FDA Inspection 780131 - Anna Jaques Hospital Laboratory - 2012-05-04 — classification: No Action Indicated (NAI), source: FDA, date: May 4, 2012
- [FDA Inspection 717231 - Anna Jaques Hospital Laboratory - 2011-03-30](https://www.keypedia.com/records/fda_inspections/anna-jaques-hospital-laboratory/c576071d-9877-4f82-8352-018185ebd8e1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 30, 2011
- FDA Inspection 605630 - Anna Jaques Hospital Laboratory - 2009-08-18 — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2009

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