# Sciarra Laboratories, Inc. – FDA Inspection, Mar 29, 2018

Source: https://www.keypedia.com/records/fda_inspections/sciarra-laboratories-inc/93380b86-d4be-4624-adb0-b4f3320c0464
Source feed: FDA_Inspections

> FDA inspection 1046128 of Sciarra Laboratories, Inc., March 29, 2018. Classification: No Action Indicated (NAI). 4 citations under 21 CFR part 820. Form 483 issued. 10 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1046128
- Company Name: Sciarra Laboratories, Inc.
- Inspection Date: 2018-03-29
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1211562 - 2023-08-07](https://www.keypedia.com/records/fda_inspections/sciarra-laboratories-inc/8cda42d2-1518-41f1-9d52-7cb809baa777)
- FDA Inspection 1041616 - 2018-02-14
- FDA Inspection 925624 - 2015-05-05
- FDA Inspection 867806 - 2014-02-07
- FDA Inspection 802381 - 2012-10-04

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jacqueline-s-warner/d001f4ec-db46-4d78-a5dd-efea7ddfb893)

Company: https://www.keypedia.com/companies/sciarra-laboratories-inc/524d2f58-5717-46af-bdb2-7289f54a823d

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7