# AstraZeneca UK Ltd. - Inspection Records

Source: https://www.keypedia.com/companies/astrazeneca-uk-ltd/d28c6a70-76f3-49fb-a3c2-bc412f662941

> Inspection records and compliance data for AstraZeneca UK Ltd. in Macclesfield, None. Access full analysis and detailed observations.

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## Details

- Name: AstraZeneca UK Ltd.
- FEI Number: 3002850317
- City: Macclesfield
- State: None
- Country Name: United Kingdom
- Address Line 1: Charter Way, Silk Road Business Park
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1274179 - AstraZeneca UK Ltd. - 2023-04-27](https://www.keypedia.com/records/fda_inspections/astrazeneca-uk-ltd/6a8532df-72b5-4d04-95c8-cbc92847ca5b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 27, 2023
- [FDA Inspection 1129231 - AstraZeneca UK Ltd. - 2020-02-23](https://www.keypedia.com/records/fda_inspections/astrazeneca-uk-ltd/3fac1cfc-478e-4bfb-93a9-32377a244321) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 23, 2020
- [FDA Inspection 1017549 - AstraZeneca UK Ltd. - 2017-04-13](https://www.keypedia.com/records/fda_inspections/astrazeneca-uk-ltd/2a1cf33a-fc30-4b92-af4c-d0acf92b6952) — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2017
- [FDA Inspection 878183 - AstraZeneca UK Ltd. - 2014-04-11](https://www.keypedia.com/records/fda_inspections/astrazeneca-uk-ltd/8cc74265-2638-4a52-94ce-5253cd0fe142) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 11, 2014
- [FDA Inspection 785250 - AstraZeneca UK Ltd. - 2012-03-16](https://www.keypedia.com/records/fda_inspections/astrazeneca-uk-ltd/c572832d-302e-402a-84aa-5194f7ad10d9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 16, 2012
- [FDA Inspection 612417 - AstraZeneca UK Ltd. - 2009-08-14](https://www.keypedia.com/records/fda_inspections/astrazeneca-uk-ltd/38cd0e2c-9dd9-4b44-8baf-79fe438e34b3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 14, 2009

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