# Xela Pack, Inc, Saline, MI – FDA Inspections

Source: https://www.keypedia.com/companies/xela-pack-inc/14aef6c6-35ac-4d24-bb2f-34aa7e952b6e

> Inspection records and compliance data for Xela Pack, Inc in Saline, Michigan. 7 FDA inspections on record, 1 Form 483, last inspected February 09, 2023.

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## Details

- Name: Xela Pack, Inc
- FEI Number: 1832962
- Address Line 1: 8300 Boettner Rd
- City: Saline
- State: Michigan
- Zip Code: 48176
- Country Name: United States
- Address: 8300 Boettner Rd, Saline, Michigan 48176, United States
- Country: United States

## Related Documents

- FDA Inspection 1197487 - Xela Pack, Inc - 2023-02-09 — source: FDA, date: February 9, 2023
- FDA Inspection 1079243 - Xela Pack, Inc - 2019-02-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 7, 2019
- [FDA Inspection 1079243 - Xela Pack, Inc - 2019-02-07](https://www.keypedia.com/records/fda_inspections/xela-pack-inc/e97f02fb-7cc3-422a-83fc-f5fef4a198e2) — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2019
- FDA Inspection 961854 - Xela Pack, Inc - 2015-12-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 22, 2015
- FDA Inspection 961854 - Xela Pack, Inc - 2015-12-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 22, 2015
- [FDA Inspection 820583 - Xela Pack, Inc - 2013-03-01](https://www.keypedia.com/records/fda_inspections/xela-pack-inc/ea88f508-81af-4552-8008-4336a59b8ac8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 1, 2013
- FDA Inspection 820583 - Xela Pack, Inc - 2013-03-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 1, 2013
- FDA Inspection 820583 - Xela Pack, Inc - 2013-03-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 1, 2013
- FDA Inspection 764320 - Xela Pack, Inc - 2012-01-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 24, 2012
- FDA Inspection 764320 - Xela Pack, Inc - 2012-01-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 24, 2012

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