# Mylan Teoranta, Inverin, Ireland – FDA Inspections

Source: https://www.keypedia.com/companies/mylan-teoranta/070856c0-ee70-4d73-a354-2afd7aa24c14

> Inspection records and compliance data for Mylan Teoranta in Inverin. 7 FDA inspections on record, 1 Form 483, last inspected July 15, 2022.

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## Details

- Name: Mylan Teoranta
- FEI Number: 3002806521
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK
- Address Line 1: Kilroe East, Inverin
- City: Inverin
- Country Name: Ireland
- Address: Kilroe East, Inverin, Inverin, Ireland
- Country: Ireland

## Related Documents

- FDA Inspection 1202025 - Mylan Teoranta - 2022-07-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 15, 2022
- FDA Inspection 1123541 - Mylan Teoranta - 2018-06-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 22, 2018
- [FDA Inspection 1041657 - Mylan Teoranta - 2018-02-16](https://www.keypedia.com/records/fda_inspections/mylan-teoranta/af6aed52-4b5e-4a40-8994-3c57e1737204) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 16, 2018
- FDA Inspection 978312 - Mylan Teoranta - 2016-06-15 — classification: No Action Indicated (NAI), source: FDA, date: June 15, 2016
- [FDA Inspection 886146 - Mylan Teoranta - 2014-05-27](https://www.keypedia.com/records/fda_inspections/mylan-teoranta/b043bac6-5e98-4334-9237-2d1fd03c5f93) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 27, 2014
- FDA Inspection 782346 - Mylan Teoranta - 2012-03-30 — classification: No Action Indicated (NAI), source: FDA, date: March 30, 2012
- FDA Inspection 628714 - Mylan Teoranta - 2009-10-15 — classification: No Action Indicated (NAI), source: FDA, date: October 15, 2009

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