Facility

PRECISION DYNAMICS CORPORATION

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

1inspections · worst NAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	2020282
Establishment type	Complaint File Establishment per 21 CFR 820.198
Location	25124 Springfield Ct Ste 200 Valencia, CA, US 91355
Registration status	Active · expires 2026
Parent company	Precision Dynamics Corporation (owner-operator 2020282)
Brand names	Sterile Medication Labels

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Label Or Tag, Sterile
Product code LYV (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4800

Recalls & enforcement

Class IITerminated2013-07-10
PDC Healthcare initiated this recall of Non-Sterile Viscot Part Number 1437-100 Surgical Skin Markers, becuase they were inadvertently mislabeled as PN STER-VIS Sterile Skin Marker Pen with Labels and Flex Ruter.

FDA inspections (1)

NAI2016-01-27
No Action Indicated · Compliance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “PRECISION DYNAMICS CORPORATION (FEI 2020282) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2020282-precision-dynamics-corporation/

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