# ACell, Inc - Inspection Records

Source: https://www.globalkeysolutions.net/companies/acell-inc/278a3150-6c2b-4a18-8806-7145ea4395b9

> Inspection records and compliance data for ACell, Inc in Columbia, Maryland. Access full analysis and detailed observations.

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## Details

- Name: ACell, Inc
- FEI Number: 3005920706
- City: Columbia
- State: Maryland
- Country Name: United States
- Address Line 1: 6640 Eli Whitney Dr Ste 200
- Zip Code: 21046

## Related Documents

- [FDA Inspection 966729 - ACell, Inc - 2016-03-08](https://www.globalkeysolutions.net/records/fda_inspections/acell-inc/1bb8436a-d68f-4d57-a6e9-6379c35b487d) — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2016
- [FDA Inspection 856079 - ACell, Inc - 2013-11-20](https://www.globalkeysolutions.net/records/fda_inspections/acell-inc/22a96c0c-5aff-43bc-844c-f108966328de) — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2013
- [WARNING_LETTER - ACell, Inc - 2012-12-20](https://www.globalkeysolutions.net/records/warning_letter/acell-inc/0ab58bcc-9829-4937-b5a0-cc96b3f59a2f) — source: FDA, date: December 20, 2012
- [FDA Inspection 811984 - ACell, Inc - 2012-12-20](https://www.globalkeysolutions.net/records/fda_inspections/acell-inc/00fc9876-03c8-4578-b6bc-291ab920cd36) — classification: Official Action Indicated (OAI), source: FDA, date: December 20, 2012
- [FDA Inspection 811984 - ACell, Inc - 2012-12-20](https://www.globalkeysolutions.net/records/fda_inspections/acell-inc/a751a08c-3361-4b42-8dd6-a4761d6cb72e) — classification: Official Action Indicated (OAI), source: FDA, date: December 20, 2012
- [FDA Inspection 643284 - ACell, Inc - 2010-02-03](https://www.globalkeysolutions.net/records/fda_inspections/acell-inc/ff937155-de59-4952-8905-1e1febb49e4b) — classification: No Action Indicated (NAI), source: FDA, date: February 3, 2010
- [FDA Inspection 643284 - ACell, Inc - 2010-02-03](https://www.globalkeysolutions.net/records/fda_inspections/acell-inc/a55b99d9-17f4-4564-8f4b-d532b349b03a) — classification: No Action Indicated (NAI), source: FDA, date: February 3, 2010

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## Related Officers

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