FDA Inspection
Celestica CorporationCelestica Corporation – FDA Inspection, Nov 12, 2008
Record Details
This FDA Inspection record concerns Celestica Corporation, with an inspection on November 12, 2008, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Celestica Corporation
- Inspection Date
- November 12, 2008
- Product Type
- Devices
View Company Profile
ID · 7269cd33-ac9b-4308-a401-d46750b6cc23
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 547539
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.20(c)Management review participants
- 21 CFR 820.25(b)Training
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.90(b)(1)Documentation of disposition, justification, signature
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