FDA Inspection
Handheld Products, Inc., dba Honeywell Scanning and MobilityHandheld Products, Inc., dba Honeywell Scanning and Mobility – FDA Inspection, Mar 2, 2009
Record Details
This FDA Inspection record concerns Handheld Products, Inc., dba Honeywell Scanning and Mobility, with an inspection on March 2, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 2, 2009
- Product Type
- Devices
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ID · a2a678c3-f388-4956-b2de-d8a7c19652ca
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 570043
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
- 21 CFR 820.90(a)Specific non-conforming product procedures
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