# Straumann USA LLC, Andover, MA – FDA Inspections

Source: https://www.keypedia.com/companies/straumann-usa-llc/9a27e5b2-2d25-4a71-a1d2-0cfda8b41aa0

> Inspection records and compliance data for Straumann USA LLC in Andover, Massachusetts. 4 FDA inspections on record, 1 Form 483, last inspected March 04, 2020.

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## Details

- Name: Straumann USA LLC
- FEI Number: 1000121052
- Address Line 1: 60 Minuteman Rd
- City: Andover
- State: Massachusetts
- Zip Code: 01810
- Country Name: United States
- Address: 60 Minuteman Rd, Andover, Massachusetts 01810, United States
- Country: United States

## Related Documents

- FDA Inspection 1122746 - Straumann USA LLC - 2020-03-04 — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2020
- FDA Inspection 1122746 - Straumann USA LLC - 2020-03-04 — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2020
- FDA Inspection 1122746 - Straumann USA LLC - 2020-03-04 — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2020
- FDA Inspection 1019048 - Straumann USA LLC - 2017-07-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2017
- [FDA Inspection 1019048 - Straumann USA LLC - 2017-07-21](https://www.keypedia.com/records/fda_inspections/straumann-usa-llc/f57f061c-13d5-4966-9105-ff7700d6a182) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2017
- FDA Inspection 1019048 - Straumann USA LLC - 2017-07-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2017
- FDA Inspection 1019048 - Straumann USA LLC - 2017-07-21 — classification: No Action Indicated (NAI), source: FDA, date: July 21, 2017
- FDA Inspection 903433 - Straumann USA LLC - 2014-11-13 — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2014
- FDA Inspection 903595 - Straumann USA LLC - 2014-11-13 — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2014
- FDA Inspection 903433 - Straumann USA LLC - 2014-11-13 — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2014

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